Canonical Allele Identifier: CA346730077

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1509993
• ClinVar RCV Id: RCV002011435
• dbSNP Id: rs2104406360
• MyVariant Identifiers: chr2:g.47705574A>T (hg19) ; chr2:g.47478435A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478435A>T , CM000664.2:g.47478435A>T	GRCh38
NC_000002.11:g.47705574A>T , CM000664.1:g.47705574A>T	GRCh37
NC_000002.10:g.47559078A>T	NCBI36
NG_007110.2:g.80312A>T , LRG_218:g.80312A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.2374A>T	ENSP00000495641.2:p.Asn792Tyr
ENST00000233146.7:c.2374A>T MANE Select	ENSP00000233146.2:p.Asn792Tyr
ENST00000543555.6:c.2176A>T	ENSP00000442697.1:p.Asn726Tyr
ENST00000644092.1:c.*674A>T	ENSP00000496351.1:n.*674A>T
ENST00000644900.1:c.227A>T
ENST00000645339.1:c.2374A>T	ENSP00000496441.1:p.Asn792Tyr
ENST00000645506.1:c.2374A>T	ENSP00000495455.1:p.Asn792Tyr
ENST00000646415.1:c.2374A>T	ENSP00000495543.1:p.Asn792Tyr
ENST00000233146.6:c.2374A>T	ENSP00000233146.2:p.Asn792Tyr
ENST00000406134.5:c.2374A>T	ENSP00000384199.1:p.Asn792Tyr
ENST00000543555.5:c.2176A>T	ENSP00000442697.1:p.Asn726Tyr
ENST00000610696.4:c.*770A>T	ENSP00000483159.1:n.*770A>T
ENST00000613514.4:c.*914A>T	ENSP00000484137.1:n.*914A>T
ENST00000617333.3:c.*1140A>T	ENSP00000482468.1:n.*1140A>T
ENST00000617938.4:c.*1346A>T	ENSP00000481158.1:n.*1346A>T
ENST00000621359.2:c.2373A>T	ENSP00000481416.1:p.Pro791=
NM_000251.2:c.2374A>T , LRG_218t1:c.2374A>T	NP_000242.1:p.Asn792Tyr
NM_001258281.1:c.2176A>T	NP_001245210.1:p.Asn726Tyr
XM_005264332.2:c.2374A>T	XP_005264389.2:p.Asn792Tyr
XM_011532867.1:c.2374A>T	XP_011531169.1:p.Asn792Tyr
XR_939685.1:n.2446A>T
XM_005264332.4:c.2374A>T	XP_005264389.2:p.Asn792Tyr
XM_011532867.2:c.2374A>T	XP_011531169.1:p.Asn792Tyr
XR_001738747.2:n.2436A>T
XR_939685.2:n.2436A>T
NM_000251.3:c.2374A>T MANE Select	NP_000242.1:p.Asn792Tyr