Canonical Allele Identifier: CA346729963

Gene: MSH2

Linked Data

• dbSNP Id: rs1553369750
• MyVariant Identifiers: chr2:g.47705550T>A (hg19) ; chr2:g.47478411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47478411T>A , CM000664.2:g.47478411T>A	GRCh38
NC_000002.11:g.47705550T>A , CM000664.1:g.47705550T>A	GRCh37
NC_000002.10:g.47559054T>A	NCBI36
NG_007110.2:g.80288T>A , LRG_218:g.80288T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2350T>A	ENSP00000495641.2:p.Phe784Ile
ENST00000233146.7:c.2350T>A MANE Select	ENSP00000233146.2:p.Phe784Ile
ENST00000543555.6:c.2152T>A	ENSP00000442697.1:p.Phe718Ile
ENST00000644092.1:c.*650T>A	ENSP00000496351.1:n.*650T>A
ENST00000644900.1:c.203T>A
ENST00000645339.1:c.2350T>A	ENSP00000496441.1:p.Phe784Ile
ENST00000645506.1:c.2350T>A	ENSP00000495455.1:p.Phe784Ile
ENST00000646415.1:c.2350T>A	ENSP00000495543.1:p.Phe784Ile
ENST00000233146.6:c.2350T>A	ENSP00000233146.2:p.Phe784Ile
ENST00000406134.5:c.2350T>A	ENSP00000384199.1:p.Phe784Ile
ENST00000543555.5:c.2152T>A	ENSP00000442697.1:p.Phe718Ile
ENST00000610696.4:c.*746T>A	ENSP00000483159.1:n.*746T>A
ENST00000613514.4:c.*890T>A	ENSP00000484137.1:n.*890T>A
ENST00000617333.3:c.*1116T>A	ENSP00000482468.1:n.*1116T>A
ENST00000617938.4:c.*1322T>A	ENSP00000481158.1:n.*1322T>A
ENST00000621359.2:c.2349T>A	ENSP00000481416.1:p.Ile783=
NM_000251.2:c.2350T>A , LRG_218t1:c.2350T>A	NP_000242.1:p.Phe784Ile
NM_001258281.1:c.2152T>A	NP_001245210.1:p.Phe718Ile
XM_005264332.2:c.2350T>A	XP_005264389.2:p.Phe784Ile
XM_011532867.1:c.2350T>A	XP_011531169.1:p.Phe784Ile
XR_939685.1:n.2422T>A
XM_005264332.4:c.2350T>A	XP_005264389.2:p.Phe784Ile
XM_011532867.2:c.2350T>A	XP_011531169.1:p.Phe784Ile
XR_001738747.2:n.2412T>A
XR_939685.2:n.2412T>A
NM_000251.3:c.2350T>A MANE Select	NP_000242.1:p.Phe784Ile