Canonical Allele Identifier: CA366735789

Gene: PMS2

Linked Data

• MyVariant Identifiers: chr7:g.6017292C>A (hg19) ; chr7:g.5977661C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5977661C>A , CM000669.2:g.5977661C>A	GRCh38
NC_000007.13:g.6017292C>A , CM000669.1:g.6017292C>A	GRCh37
NC_000007.12:g.5983818C>A	NCBI36
NG_008466.1:g.36446G>T , LRG_161:g.36446G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1768G>T	ENSP00000514615.2:n.*1768G>T
ENST00000699840.2:c.2369G>T	ENSP00000514638.2:p.Ser790Ile
ENST00000699930.2:c.2264G>T	ENSP00000514695.2:p.Ser755Ile
ENST00000406569.8:c.1732G>T	ENSP00000514464.1:n.1732G>T
ENST00000644110.2:c.*1966G>T	ENSP00000496392.2:n.*1966G>T
ENST00000699752.1:c.2216G>T	ENSP00000514561.1:p.Ser739Ile
ENST00000699753.1:c.*1793G>T	ENSP00000514562.1:n.*1793G>T
ENST00000699754.1:c.2174G>T	ENSP00000514563.1:p.Ser725Ile
ENST00000699755.1:c.*1771G>T	ENSP00000514564.1:n.*1771G>T
ENST00000699756.1:c.*1959G>T	ENSP00000514565.1:n.*1959G>T
ENST00000699757.1:c.*1629G>T	ENSP00000514566.1:n.*1629G>T
ENST00000699758.1:c.*1629G>T	ENSP00000514567.1:n.*1629G>T
ENST00000699759.1:n.3226G>T
ENST00000699760.1:c.2054G>T	ENSP00000514568.1:p.Ser685Ile
ENST00000699761.1:c.1967G>T	ENSP00000514569.1:p.Ser656Ile
ENST00000699762.1:c.1799G>T	ENSP00000514570.1:p.Ser600Ile
ENST00000699763.1:c.*1462G>T	ENSP00000514571.1:n.*1462G>T
ENST00000699764.1:c.*690G>T	ENSP00000514572.1:n.*690G>T
ENST00000699765.1:c.*1367G>T	ENSP00000514573.1:n.*1367G>T
ENST00000699766.1:c.2405G>T	ENSP00000514574.1:p.Ser802Ile
ENST00000699767.1:c.*13G>T	ENSP00000514575.1:n.*13G>T
ENST00000699768.1:c.2228G>T	ENSP00000514576.1:p.Ser743Ile
ENST00000699811.1:c.1967G>T	ENSP00000514614.1:p.Ser656Ile
ENST00000699813.1:n.2485G>T
ENST00000699814.1:c.1995G>T
ENST00000699815.1:c.*1903G>T	ENSP00000514616.1:n.*1903G>T
ENST00000699816.1:c.*1262G>T	ENSP00000514617.1:n.*1262G>T
ENST00000699817.1:c.*1966G>T	ENSP00000514618.1:n.*1966G>T
ENST00000699818.1:c.1967G>T	ENSP00000514619.1:p.Ser656Ile
ENST00000699819.1:c.*1529G>T	ENSP00000514620.1:n.*1529G>T
ENST00000699820.1:c.*310G>T	ENSP00000514621.1:n.*310G>T
ENST00000699821.1:c.2000G>T	ENSP00000514622.1:p.Ser667Ile
ENST00000699822.1:c.*1824G>T	ENSP00000514623.1:n.*1824G>T
ENST00000699823.1:c.1967G>T	ENSP00000514624.1:p.Ser656Ile
ENST00000699824.1:c.*1875G>T	ENSP00000514625.1:n.*1875G>T
ENST00000699825.1:c.1811G>T	ENSP00000514626.1:p.Ser604Ile
ENST00000699826.1:c.*1771G>T	ENSP00000514627.1:n.*1771G>T
ENST00000699827.1:c.2204G>T	ENSP00000514628.1:p.Ser735Ile
ENST00000699828.1:c.*1462G>T	ENSP00000514629.1:n.*1462G>T
ENST00000699833.1:n.4144G>T
ENST00000699837.1:c.1967G>T	ENSP00000514635.1:p.Ser656Ile
ENST00000699838.1:c.*2272G>T	ENSP00000514636.1:n.*2272G>T
ENST00000699839.1:c.2558G>T	ENSP00000514637.1:p.Ser853Ile
ENST00000699916.1:c.*1629G>T	ENSP00000514684.1:n.*1629G>T
ENST00000699917.1:c.*1821G>T	ENSP00000514685.1:n.*1821G>T
ENST00000699918.1:c.*1873G>T	ENSP00000514686.1:n.*1873G>T
ENST00000699919.1:c.*1959G>T	ENSP00000514687.1:n.*1959G>T
ENST00000699920.1:c.*2008G>T	ENSP00000514688.1:n.*2008G>T
ENST00000699928.1:c.*310G>T	ENSP00000514693.1:n.*310G>T
ENST00000699951.1:c.*1425G>T	ENSP00000514706.1:n.*1425G>T
ENST00000699952.1:c.804-4119G>T	ENSP00000514707.1:n.804-4119G>T
ENST00000265849.12:c.2372G>T MANE Select	ENSP00000265849.7:p.Ser791Ile
ENST00000642292.1:c.1967G>T	ENSP00000495524.1:p.Ser656Ile
ENST00000642456.1:c.1967G>T	ENSP00000493814.1:p.Ser656Ile
ENST00000643595.1:c.*1771G>T	ENSP00000494497.1:n.*1771G>T
ENST00000644110.1:c.2054G>T	ENSP00000496392.1:p.Ser685Ile
ENST00000265849.11:c.2372G>T	ENSP00000265849.7:p.Ser791Ile
ENST00000382321.5:c.1169G>T	ENSP00000371758.4:p.Ser390Ile
ENST00000441476.6:c.2054G>T	ENSP00000392843.2:p.Ser685Ile
NM_000535.5:c.2372G>T , LRG_161t1:c.2372G>T	NP_000526.1:p.Ser791Ile
NR_003085.2:n.2454G>T
XM_006715742.2:c.2366G>T	XP_006715805.1:p.Ser789Ile
XM_006715744.2:c.1439G>T	XP_006715807.1:p.Ser480Ile
XM_011515427.1:c.2417G>T	XP_011513729.1:p.Ser806Ile
XM_011515428.1:c.2261G>T	XP_011513730.1:p.Ser754Ile
XM_011515429.1:c.2054G>T	XP_011513731.1:p.Ser685Ile
XM_011515430.1:c.2054G>T	XP_011513732.1:p.Ser685Ile
NM_000535.6:c.2372G>T	NP_000526.2:p.Ser791Ile
NM_001322003.1:c.1967G>T	NP_001308932.1:p.Ser656Ile
NM_001322004.1:c.1967G>T	NP_001308933.1:p.Ser656Ile
NM_001322005.1:c.1967G>T	NP_001308934.1:p.Ser656Ile
NM_001322006.1:c.2216G>T	NP_001308935.1:p.Ser739Ile
NM_001322007.1:c.2054G>T	NP_001308936.1:p.Ser685Ile
NM_001322008.1:c.2054G>T	NP_001308937.1:p.Ser685Ile
NM_001322009.1:c.2000G>T	NP_001308938.1:p.Ser667Ile
NM_001322010.1:c.1811G>T	NP_001308939.1:p.Ser604Ile
NM_001322011.1:c.1439G>T	NP_001308940.1:p.Ser480Ile
NM_001322012.1:c.1439G>T	NP_001308941.1:p.Ser480Ile
NM_001322013.1:c.1799G>T	NP_001308942.1:p.Ser600Ile
NM_001322014.1:c.2405G>T	NP_001308943.1:p.Ser802Ile
NM_001322015.1:c.2063G>T	NP_001308944.1:p.Ser688Ile
NR_136154.1:n.2416G>T
XM_006715744.4:c.1439G>T	XP_006715807.1:p.Ser480Ile
XM_017012342.2:c.1439G>T	XP_016867831.1:p.Ser480Ile
XM_024446800.1:c.1811G>T	XP_024302568.1:p.Ser604Ile
NM_000535.7:c.2372G>T MANE Select	NP_000526.2:p.Ser791Ile
NM_001322003.2:c.1967G>T	NP_001308932.1:p.Ser656Ile
NM_001322004.2:c.1967G>T	NP_001308933.1:p.Ser656Ile
NM_001322005.2:c.1967G>T	NP_001308934.1:p.Ser656Ile
NM_001322006.2:c.2216G>T	NP_001308935.1:p.Ser739Ile
NM_001322008.2:c.2054G>T	NP_001308937.1:p.Ser685Ile
NM_001322009.2:c.2000G>T	NP_001308938.1:p.Ser667Ile
NM_001322010.2:c.1811G>T	NP_001308939.1:p.Ser604Ile
NM_001322011.2:c.1439G>T	NP_001308940.1:p.Ser480Ile
NM_001322012.2:c.1439G>T	NP_001308941.1:p.Ser480Ile
NM_001322013.2:c.1799G>T	NP_001308942.1:p.Ser600Ile
NM_001322014.2:c.2405G>T	NP_001308943.1:p.Ser802Ile
NM_001322015.2:c.2063G>T	NP_001308944.1:p.Ser688Ile
NM_001322007.2:c.2054G>T	NP_001308936.1:p.Ser685Ile