Canonical Allele Identifier: CA2495832718

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412475_47412482delinsACATTTAT , CM000664.2:g.47412475_47412482delinsACATTTAT	GRCh38
NC_000002.11:g.47639614_47639621delinsACATTTAT , CM000664.1:g.47639614_47639621delinsACATTTAT	GRCh37
NC_000002.10:g.47493118_47493125delinsACATTTAT	NCBI36
NG_007110.2:g.14352_14359delinsACATTTAT , LRG_218:g.14352_14359delinsACATTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.707_714delinsACATTTAT	ENSP00000495641.2:p.Asp236=
ENST00000233146.7:c.707_714delinsACATTTAT MANE Select	ENSP00000233146.2:p.Asp236=
ENST00000543555.6:c.509_516delinsACATTTAT	ENSP00000442697.1:p.Asp170=
ENST00000644092.1:c.707_714delinsACATTTAT	ENSP00000496351.1:p.Asp236=
ENST00000645339.1:c.707_714delinsACATTTAT	ENSP00000496441.1:p.Asp236=
ENST00000645506.1:c.707_714delinsACATTTAT	ENSP00000495455.1:p.Asp236=
ENST00000646415.1:c.707_714delinsACATTTAT	ENSP00000495543.1:p.Asp236=
ENST00000233146.6:c.707_714delinsACATTTAT	ENSP00000233146.2:p.Asp236=
ENST00000406134.5:c.707_714delinsACATTTAT	ENSP00000384199.1:p.Asp236=
ENST00000543555.5:c.509_516delinsACATTTAT	ENSP00000442697.1:p.Asp170=
ENST00000610696.4:c.707_714delinsACATTTAT	ENSP00000483159.1:p.Asp236=
ENST00000613514.4:c.707_714delinsACATTTAT	ENSP00000484137.1:p.Asp236=
ENST00000617333.3:c.707_714delinsACATTTAT	ENSP00000482468.1:p.Asp236=
ENST00000617938.4:c.707_714delinsACATTTAT	ENSP00000481158.1:p.Asp236=
ENST00000621359.2:c.707_714delinsACATTTAT	ENSP00000481416.1:p.Asp236=
NM_000251.2:c.707_714delinsACATTTAT , LRG_218t1:c.707_714delinsACATTTAT	NP_000242.1:p.Asp236=
NM_001258281.1:c.509_516delinsACATTTAT	NP_001245210.1:p.Asp170=
XM_005264332.2:c.707_714delinsACATTTAT	XP_005264389.2:p.Asp236=
XM_011532867.1:c.707_714delinsACATTTAT	XP_011531169.1:p.Asp236=
XR_939685.1:n.779_786delinsACATTTAT
XM_005264332.4:c.707_714delinsACATTTAT	XP_005264389.2:p.Asp236=
XM_011532867.2:c.707_714delinsACATTTAT	XP_011531169.1:p.Asp236=
XR_001738747.2:n.769_776delinsACATTTAT
XR_939685.2:n.769_776delinsACATTTAT
NM_000251.3:c.707_714delinsACATTTAT MANE Select	NP_000242.1:p.Asp236=