Canonical Allele Identifier: CA011600

Gene: PMS2

Linked Data

• ClinVar Variation Id: 183718
• ClinVar RCV Id: RCV000162416 ; RCV000657711 ; RCV003317111 ; RCV001066692 ; RCV003454389
• dbSNP Id: rs786201039
• MyVariant Identifiers: chr7:g.6013113C>A (hg19) ; chr7:g.5973482C>A (hg38)
• PubMed: PMID:24027009

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5973482C>A , CM000669.2:g.5973482C>A	GRCh38
NC_000007.13:g.6013113C>A , CM000669.1:g.6013113C>A	GRCh37
NC_000007.12:g.5979639C>A	NCBI36
NG_008466.1:g.40625G>T , LRG_161:g.40625G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1902G>T	ENSP00000514615.2:n.*1902G>T
ENST00000699840.2:c.2503G>T	ENSP00000514638.2:p.Glu835Ter
ENST00000699930.2:c.2398G>T	ENSP00000514695.2:p.Glu800Ter
ENST00000406569.8:c.1866G>T	ENSP00000514464.1:n.1866G>T
ENST00000644110.2:c.*2100G>T	ENSP00000496392.2:n.*2100G>T
ENST00000699752.1:c.2350G>T	ENSP00000514561.1:p.Glu784Ter
ENST00000699753.1:c.*1927G>T	ENSP00000514562.1:n.*1927G>T
ENST00000699754.1:c.2308G>T	ENSP00000514563.1:p.Glu770Ter
ENST00000699755.1:c.*1905G>T	ENSP00000514564.1:n.*1905G>T
ENST00000699756.1:c.*2093G>T	ENSP00000514565.1:n.*2093G>T
ENST00000699757.1:c.*1763G>T	ENSP00000514566.1:n.*1763G>T
ENST00000699758.1:c.*1763G>T	ENSP00000514567.1:n.*1763G>T
ENST00000699759.1:n.3360G>T
ENST00000699760.1:c.2188G>T	ENSP00000514568.1:p.Glu730Ter
ENST00000699761.1:c.2101G>T	ENSP00000514569.1:p.Glu701Ter
ENST00000699762.1:c.1933G>T	ENSP00000514570.1:p.Glu645Ter
ENST00000699763.1:c.*1596G>T	ENSP00000514571.1:n.*1596G>T
ENST00000699764.1:c.*824G>T	ENSP00000514572.1:n.*824G>T
ENST00000699765.1:c.*1501G>T	ENSP00000514573.1:n.*1501G>T
ENST00000699766.1:c.2539G>T	ENSP00000514574.1:p.Glu847Ter
ENST00000699767.1:c.*147G>T	ENSP00000514575.1:n.*147G>T
ENST00000699768.1:c.2362G>T	ENSP00000514576.1:p.Glu788Ter
ENST00000699811.1:c.2101G>T	ENSP00000514614.1:p.Glu701Ter
ENST00000699813.1:n.2619G>T
ENST00000699814.1:c.2129G>T
ENST00000699815.1:c.*2037G>T	ENSP00000514616.1:n.*2037G>T
ENST00000699816.1:c.*1396G>T	ENSP00000514617.1:n.*1396G>T
ENST00000699817.1:c.*2100G>T	ENSP00000514618.1:n.*2100G>T
ENST00000699818.1:c.2101G>T	ENSP00000514619.1:p.Glu701Ter
ENST00000699819.1:c.*1663G>T	ENSP00000514620.1:n.*1663G>T
ENST00000699820.1:c.*444G>T	ENSP00000514621.1:n.*444G>T
ENST00000699821.1:c.2134G>T	ENSP00000514622.1:p.Glu712Ter
ENST00000699822.1:c.*1958G>T	ENSP00000514623.1:n.*1958G>T
ENST00000699823.1:c.2101G>T	ENSP00000514624.1:p.Glu701Ter
ENST00000699824.1:c.*2009G>T	ENSP00000514625.1:n.*2009G>T
ENST00000699825.1:c.1945G>T	ENSP00000514626.1:p.Glu649Ter
ENST00000699826.1:c.*1905G>T	ENSP00000514627.1:n.*1905G>T
ENST00000699827.1:c.2338G>T	ENSP00000514628.1:p.Glu780Ter
ENST00000699828.1:c.*1596G>T	ENSP00000514629.1:n.*1596G>T
ENST00000699833.1:n.4278G>T
ENST00000699837.1:c.2101G>T	ENSP00000514635.1:p.Glu701Ter
ENST00000699838.1:c.*2406G>T	ENSP00000514636.1:n.*2406G>T
ENST00000699839.1:c.2692G>T	ENSP00000514637.1:p.Glu898Ter
ENST00000699916.1:c.*1763G>T	ENSP00000514684.1:n.*1763G>T
ENST00000699917.1:c.*1955G>T	ENSP00000514685.1:n.*1955G>T
ENST00000699918.1:c.*2007G>T	ENSP00000514686.1:n.*2007G>T
ENST00000699919.1:c.*2093G>T	ENSP00000514687.1:n.*2093G>T
ENST00000699920.1:c.*2142G>T	ENSP00000514688.1:n.*2142G>T
ENST00000699928.1:c.*444G>T	ENSP00000514693.1:n.*444G>T
ENST00000699951.1:c.*1559G>T	ENSP00000514706.1:n.*1559G>T
ENST00000699952.1:c.*60G>T	ENSP00000514707.1:n.*60G>T
ENST00000265849.12:c.2506G>T MANE Select	ENSP00000265849.7:p.Glu836Ter
ENST00000642292.1:c.2101G>T	ENSP00000495524.1:p.Glu701Ter
ENST00000642456.1:c.2101G>T	ENSP00000493814.1:p.Glu701Ter
ENST00000643595.1:c.*1905G>T	ENSP00000494497.1:n.*1905G>T
ENST00000644110.1:c.2188G>T	ENSP00000496392.1:p.Glu730Ter
ENST00000265849.11:c.2506G>T	ENSP00000265849.7:p.Glu836Ter
ENST00000382321.5:c.1303G>T	ENSP00000371758.4:p.Glu435Ter
ENST00000441476.6:c.2188G>T	ENSP00000392843.2:p.Glu730Ter
NM_000535.5:c.2506G>T , LRG_161t1:c.2506G>T	NP_000526.1:p.Glu836Ter
NR_003085.2:n.2588G>T
XM_006715742.2:c.2500G>T	XP_006715805.1:p.Glu834Ter
XM_006715744.2:c.1573G>T	XP_006715807.1:p.Glu525Ter
XM_011515427.1:c.2551G>T	XP_011513729.1:p.Glu851Ter
XM_011515428.1:c.2395G>T	XP_011513730.1:p.Glu799Ter
XM_011515429.1:c.2188G>T	XP_011513731.1:p.Glu730Ter
XM_011515430.1:c.2188G>T	XP_011513732.1:p.Glu730Ter
NM_000535.6:c.2506G>T	NP_000526.2:p.Glu836Ter
NM_001322003.1:c.2101G>T	NP_001308932.1:p.Glu701Ter
NM_001322004.1:c.2101G>T	NP_001308933.1:p.Glu701Ter
NM_001322005.1:c.2101G>T	NP_001308934.1:p.Glu701Ter
NM_001322006.1:c.2350G>T	NP_001308935.1:p.Glu784Ter
NM_001322007.1:c.2188G>T	NP_001308936.1:p.Glu730Ter
NM_001322008.1:c.2188G>T	NP_001308937.1:p.Glu730Ter
NM_001322009.1:c.2134G>T	NP_001308938.1:p.Glu712Ter
NM_001322010.1:c.1945G>T	NP_001308939.1:p.Glu649Ter
NM_001322011.1:c.1573G>T	NP_001308940.1:p.Glu525Ter
NM_001322012.1:c.1573G>T	NP_001308941.1:p.Glu525Ter
NM_001322013.1:c.1933G>T	NP_001308942.1:p.Glu645Ter
NM_001322014.1:c.2539G>T	NP_001308943.1:p.Glu847Ter
NM_001322015.1:c.2197G>T	NP_001308944.1:p.Glu733Ter
NR_136154.1:n.2550G>T
XM_006715744.4:c.1573G>T	XP_006715807.1:p.Glu525Ter
XM_017012342.2:c.1573G>T	XP_016867831.1:p.Glu525Ter
XM_024446800.1:c.1945G>T	XP_024302568.1:p.Glu649Ter
NM_000535.7:c.2506G>T MANE Select	NP_000526.2:p.Glu836Ter
NM_001322003.2:c.2101G>T	NP_001308932.1:p.Glu701Ter
NM_001322004.2:c.2101G>T	NP_001308933.1:p.Glu701Ter
NM_001322005.2:c.2101G>T	NP_001308934.1:p.Glu701Ter
NM_001322006.2:c.2350G>T	NP_001308935.1:p.Glu784Ter
NM_001322008.2:c.2188G>T	NP_001308937.1:p.Glu730Ter
NM_001322009.2:c.2134G>T	NP_001308938.1:p.Glu712Ter
NM_001322010.2:c.1945G>T	NP_001308939.1:p.Glu649Ter
NM_001322011.2:c.1573G>T	NP_001308940.1:p.Glu525Ter
NM_001322012.2:c.1573G>T	NP_001308941.1:p.Glu525Ter
NM_001322013.2:c.1933G>T	NP_001308942.1:p.Glu645Ter
NM_001322014.2:c.2539G>T	NP_001308943.1:p.Glu847Ter
NM_001322015.2:c.2197G>T	NP_001308944.1:p.Glu733Ter
NM_001322007.2:c.2188G>T	NP_001308936.1:p.Glu730Ter