Canonical Allele Identifier: CA366737976

Gene: PMS2

Linked Data

• MyVariant Identifiers: chr7:g.6022518T>G (hg19) ; chr7:g.5982887T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5982887T>G , CM000669.2:g.5982887T>G	GRCh38
NC_000007.13:g.6022518T>G , CM000669.1:g.6022518T>G	GRCh37
NC_000007.12:g.5989044T>G	NCBI36
NG_008466.1:g.31220A>C , LRG_161:g.31220A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699814.2:c.*1507A>C	ENSP00000514615.2:n.*1507A>C
ENST00000699840.2:c.2108A>C	ENSP00000514638.2:p.Asp703Ala
ENST00000699930.2:c.2003A>C	ENSP00000514695.2:p.Asp668Ala
ENST00000406569.8:c.1678+4200A>C	ENSP00000514464.1:n.1678+4200A>C
ENST00000644110.2:c.*1705A>C	ENSP00000496392.2:n.*1705A>C
ENST00000699752.1:c.1955A>C	ENSP00000514561.1:p.Asp652Ala
ENST00000699753.1:c.*1532A>C	ENSP00000514562.1:n.*1532A>C
ENST00000699754.1:c.1913A>C	ENSP00000514563.1:p.Asp638Ala
ENST00000699755.1:c.*1510A>C	ENSP00000514564.1:n.*1510A>C
ENST00000699756.1:c.*1698A>C	ENSP00000514565.1:n.*1698A>C
ENST00000699757.1:c.*1368A>C	ENSP00000514566.1:n.*1368A>C
ENST00000699758.1:c.*1368A>C	ENSP00000514567.1:n.*1368A>C
ENST00000699759.1:n.2965A>C
ENST00000699760.1:c.1793A>C	ENSP00000514568.1:p.Asp598Ala
ENST00000699761.1:c.1706A>C	ENSP00000514569.1:p.Asp569Ala
ENST00000699762.1:c.1538A>C	ENSP00000514570.1:p.Asp513Ala
ENST00000699763.1:c.*1201A>C	ENSP00000514571.1:n.*1201A>C
ENST00000699764.1:c.*429A>C	ENSP00000514572.1:n.*429A>C
ENST00000699765.1:c.*1207A>C	ENSP00000514573.1:n.*1207A>C
ENST00000699766.1:c.2111A>C	ENSP00000514574.1:p.Asp704Ala
ENST00000699767.1:c.2111A>C	ENSP00000514575.1:p.Asp704Ala
ENST00000699768.1:c.2111A>C	ENSP00000514576.1:p.Asp704Ala
ENST00000699811.1:c.1706A>C	ENSP00000514614.1:p.Asp569Ala
ENST00000699813.1:n.2224A>C
ENST00000699814.1:c.1734A>C
ENST00000699815.1:c.*1642A>C	ENSP00000514616.1:n.*1642A>C
ENST00000699816.1:c.*1001A>C	ENSP00000514617.1:n.*1001A>C
ENST00000699817.1:c.*1705A>C	ENSP00000514618.1:n.*1705A>C
ENST00000699818.1:c.1706A>C	ENSP00000514619.1:p.Asp569Ala
ENST00000699819.1:c.*1268A>C	ENSP00000514620.1:n.*1268A>C
ENST00000699820.1:c.*49A>C	ENSP00000514621.1:n.*49A>C
ENST00000699821.1:c.1706A>C	ENSP00000514622.1:p.Asp569Ala
ENST00000699822.1:c.*1563A>C	ENSP00000514623.1:n.*1563A>C
ENST00000699823.1:c.1706A>C	ENSP00000514624.1:p.Asp569Ala
ENST00000699824.1:c.*1614A>C	ENSP00000514625.1:n.*1614A>C
ENST00000699825.1:c.1550A>C	ENSP00000514626.1:p.Asp517Ala
ENST00000699826.1:c.*1510A>C	ENSP00000514627.1:n.*1510A>C
ENST00000699827.1:c.1943A>C	ENSP00000514628.1:p.Asp648Ala
ENST00000699828.1:c.*1201A>C	ENSP00000514629.1:n.*1201A>C
ENST00000699833.1:n.3883A>C
ENST00000699837.1:c.1706A>C	ENSP00000514635.1:p.Asp569Ala
ENST00000699838.1:c.*2011A>C	ENSP00000514636.1:n.*2011A>C
ENST00000699839.1:c.2297A>C	ENSP00000514637.1:p.Asp766Ala
ENST00000699916.1:c.*1368A>C	ENSP00000514684.1:n.*1368A>C
ENST00000699917.1:c.*1560A>C	ENSP00000514685.1:n.*1560A>C
ENST00000699918.1:c.*1612A>C	ENSP00000514686.1:n.*1612A>C
ENST00000699919.1:c.*1698A>C	ENSP00000514687.1:n.*1698A>C
ENST00000699920.1:c.*1747A>C	ENSP00000514688.1:n.*1747A>C
ENST00000699928.1:c.*49A>C	ENSP00000514693.1:n.*49A>C
ENST00000699951.1:c.*1207A>C	ENSP00000514706.1:n.*1207A>C
ENST00000699952.1:c.804-9345A>C	ENSP00000514707.1:n.804-9345A>C
ENST00000265849.12:c.2111A>C MANE Select	ENSP00000265849.7:p.Asp704Ala
ENST00000642292.1:c.1706A>C	ENSP00000495524.1:p.Asp569Ala
ENST00000642456.1:c.1706A>C	ENSP00000493814.1:p.Asp569Ala
ENST00000643595.1:c.*1510A>C	ENSP00000494497.1:n.*1510A>C
ENST00000644110.1:c.1793A>C	ENSP00000496392.1:p.Asp598Ala
ENST00000265849.11:c.2111A>C	ENSP00000265849.7:p.Asp704Ala
ENST00000382321.5:c.908A>C	ENSP00000371758.4:p.Asp303Ala
ENST00000406569.7:n.1678+4200A>C
ENST00000441476.6:c.1793A>C	ENSP00000392843.2:p.Asp598Ala
ENST00000469652.1:n.81A>C
NM_000535.5:c.2111A>C , LRG_161t1:c.2111A>C	NP_000526.1:p.Asp704Ala
NR_003085.2:n.2193A>C
XM_006715742.2:c.2105A>C	XP_006715805.1:p.Asp702Ala
XM_006715744.2:c.1178A>C	XP_006715807.1:p.Asp393Ala
XM_011515427.1:c.2156A>C	XP_011513729.1:p.Asp719Ala
XM_011515428.1:c.2000A>C	XP_011513730.1:p.Asp667Ala
XM_011515429.1:c.1793A>C	XP_011513731.1:p.Asp598Ala
XM_011515430.1:c.1793A>C	XP_011513732.1:p.Asp598Ala
NM_000535.6:c.2111A>C	NP_000526.2:p.Asp704Ala
NM_001322003.1:c.1706A>C	NP_001308932.1:p.Asp569Ala
NM_001322004.1:c.1706A>C	NP_001308933.1:p.Asp569Ala
NM_001322005.1:c.1706A>C	NP_001308934.1:p.Asp569Ala
NM_001322006.1:c.1955A>C	NP_001308935.1:p.Asp652Ala
NM_001322007.1:c.1793A>C	NP_001308936.1:p.Asp598Ala
NM_001322008.1:c.1793A>C	NP_001308937.1:p.Asp598Ala
NM_001322009.1:c.1706A>C	NP_001308938.1:p.Asp569Ala
NM_001322010.1:c.1550A>C	NP_001308939.1:p.Asp517Ala
NM_001322011.1:c.1178A>C	NP_001308940.1:p.Asp393Ala
NM_001322012.1:c.1178A>C	NP_001308941.1:p.Asp393Ala
NM_001322013.1:c.1538A>C	NP_001308942.1:p.Asp513Ala
NM_001322014.1:c.2111A>C	NP_001308943.1:p.Asp704Ala
NM_001322015.1:c.1802A>C	NP_001308944.1:p.Asp601Ala
NR_136154.1:n.2198A>C
XM_006715744.4:c.1178A>C	XP_006715807.1:p.Asp393Ala
XM_017012342.2:c.1178A>C	XP_016867831.1:p.Asp393Ala
XM_024446800.1:c.1550A>C	XP_024302568.1:p.Asp517Ala
NM_000535.7:c.2111A>C MANE Select	NP_000526.2:p.Asp704Ala
NM_001322003.2:c.1706A>C	NP_001308932.1:p.Asp569Ala
NM_001322004.2:c.1706A>C	NP_001308933.1:p.Asp569Ala
NM_001322005.2:c.1706A>C	NP_001308934.1:p.Asp569Ala
NM_001322006.2:c.1955A>C	NP_001308935.1:p.Asp652Ala
NM_001322008.2:c.1793A>C	NP_001308937.1:p.Asp598Ala
NM_001322009.2:c.1706A>C	NP_001308938.1:p.Asp569Ala
NM_001322010.2:c.1550A>C	NP_001308939.1:p.Asp517Ala
NM_001322011.2:c.1178A>C	NP_001308940.1:p.Asp393Ala
NM_001322012.2:c.1178A>C	NP_001308941.1:p.Asp393Ala
NM_001322013.2:c.1538A>C	NP_001308942.1:p.Asp513Ala
NM_001322014.2:c.2111A>C	NP_001308943.1:p.Asp704Ala
NM_001322015.2:c.1802A>C	NP_001308944.1:p.Asp601Ala
NM_001322007.2:c.1793A>C	NP_001308936.1:p.Asp598Ala