Canonical Allele Identifier: CA2580066865

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1755734
• ClinVar RCV Id: RCV002362067

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412452_47412455del , CM000664.2:g.47412452_47412455del	GRCh38
NC_000002.11:g.47639591_47639594del , CM000664.1:g.47639591_47639594del	GRCh37
NC_000002.10:g.47493095_47493098del	NCBI36
NG_007110.2:g.14329_14332del , LRG_218:g.14329_14332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.684_687del	ENSP00000495641.2:p.Lys229LeufsTer16
ENST00000233146.7:c.684_687del MANE Select	ENSP00000233146.2:p.Lys229LeufsTer16
ENST00000543555.6:c.486_489del	ENSP00000442697.1:p.Lys163LeufsTer16
ENST00000644092.1:c.684_687del	ENSP00000496351.1:p.Lys229LeufsTer16
ENST00000645339.1:c.684_687del	ENSP00000496441.1:p.Lys229LeufsTer16
ENST00000645506.1:c.684_687del	ENSP00000495455.1:p.Lys229LeufsTer16
ENST00000646415.1:c.684_687del	ENSP00000495543.1:p.Lys229LeufsTer16
ENST00000233146.6:c.684_687del	ENSP00000233146.2:p.Lys229LeufsTer16
ENST00000406134.5:c.684_687del	ENSP00000384199.1:p.Lys229LeufsTer16
ENST00000543555.5:c.486_489del	ENSP00000442697.1:p.Lys163LeufsTer16
ENST00000610696.4:c.684_687del	ENSP00000483159.1:p.Lys229LeufsTer16
ENST00000613514.4:c.684_687del	ENSP00000484137.1:p.Lys229LeufsTer16
ENST00000617333.3:c.684_687del	ENSP00000482468.1:p.Lys229LeufsTer16
ENST00000617938.4:c.684_687del	ENSP00000481158.1:p.Lys229LeufsTer16
ENST00000621359.2:c.684_687del	ENSP00000481416.1:p.Lys229LeufsTer16
NM_000251.2:c.684_687del , LRG_218t1:c.684_687del	NP_000242.1:p.Lys229LeufsTer16
NM_001258281.1:c.486_489del	NP_001245210.1:p.Lys163LeufsTer16
XM_005264332.2:c.684_687del	XP_005264389.2:p.Lys229LeufsTer16
XM_011532867.1:c.684_687del	XP_011531169.1:p.Lys229LeufsTer16
XR_939685.1:n.756_759del
XM_005264332.4:c.684_687del	XP_005264389.2:p.Lys229LeufsTer16
XM_011532867.2:c.684_687del	XP_011531169.1:p.Lys229LeufsTer16
XR_001738747.2:n.746_749del
XR_939685.2:n.746_749del
NM_000251.3:c.684_687del MANE Select	NP_000242.1:p.Lys229LeufsTer16