Canonical Allele Identifier: CA2495826469

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403135G= , CM000664.2:g.47403135G=	GRCh38
NC_000002.11:g.47630274G= , CM000664.1:g.47630274G=	GRCh37
NC_000002.10:g.47483778G=	NCBI36
NG_007110.2:g.5012G= , LRG_218:g.5012G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000543555.6:c.-71G=	ENSP00000442697.1:n.-71G=
ENST00000644092.1:c.-57G=	ENSP00000496351.1:n.-57G=
ENST00000645339.1:c.-57G=	ENSP00000496441.1:n.-57G=
ENST00000645506.1:c.-57G=	ENSP00000495455.1:n.-57G=
ENST00000646415.1:c.-57G=	ENSP00000495543.1:n.-57G=
ENST00000233146.6:c.-57G=	ENSP00000233146.2:n.-57G=
ENST00000406134.5:c.-57G=	ENSP00000384199.1:n.-57G=
ENST00000454849.5:c.-71G=	ENSP00000411482.1:n.-71G=
ENST00000543555.5:c.-71G=	ENSP00000442697.1:n.-71G=
NM_000251.2:c.-57G= , LRG_218t1:c.-57G=	NP_000242.1:n.-57G=
NM_001258281.1:c.-71G=	NP_001245210.1:n.-71G=
XM_005264332.2:c.-57G=	XP_005264389.2:n.-57G=
XM_011532867.1:c.-57G=	XP_011531169.1:n.-57G=
XR_939685.1:n.16G=
XM_005264332.4:c.-57G=	XP_005264389.2:n.-57G=
XM_011532867.2:c.-57G=	XP_011531169.1:n.-57G=
XR_001738747.2:n.6G=
XR_939685.2:n.6G=