Canonical Allele Identifier: CA2699270308

Gene: MSH2

Linked Data

• dbSNP Id: rs2104381070

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47476631_47476632insTCTAAAGATAGAG , CM000664.2:g.47476631_47476632insTCTAAAGATAGAG	GRCh38
NC_000002.11:g.47703770_47703771insTCTAAAGATAGAG , CM000664.1:g.47703770_47703771insTCTAAAGATAGAG	GRCh37
NC_000002.10:g.47557274_47557275insTCTAAAGATAGAG	NCBI36
NG_007110.2:g.78508_78509insTCTAAAGATAGAG , LRG_218:g.78508_78509insTCTAAAGATAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000495641.2:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000233146.7:c.2210+60_2210+61insTCTAAAGATAGAG MANE Select	ENSP00000233146.2:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000543555.6:c.2012+60_2012+61insTCTAAAGATAGAG	ENSP00000442697.1:n.2012+60_2012+61insTCTAAAGATAGAG
ENST00000644092.1:c.*510+60_*510+61insTCTAAAGATAGAG	ENSP00000496351.1:n.*510+60_*510+61insTCTAAAGATAGAG
ENST00000644900.1:c.63+60_63+61insTCTAAAGATAGAG
ENST00000645339.1:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000496441.1:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000645506.1:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000495455.1:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000646415.1:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000495543.1:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000233146.6:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000233146.2:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000406134.5:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000384199.1:n.2210+60_2210+61insTCTAAAGATAGAG
ENST00000543555.5:c.2012+60_2012+61insTCTAAAGATAGAG	ENSP00000442697.1:n.2012+60_2012+61insTCTAAAGATAGAG
ENST00000610696.4:c.*606+60_*606+61insTCTAAAGATAGAG	ENSP00000483159.1:n.*606+60_*606+61insTCTAAAGATAGAG
ENST00000613514.4:c.*750+60_*750+61insTCTAAAGATAGAG	ENSP00000484137.1:n.*750+60_*750+61insTCTAAAGATAGAG
ENST00000617333.3:c.*976+60_*976+61insTCTAAAGATAGAG	ENSP00000482468.1:n.*976+60_*976+61insTCTAAAGATAGAG
ENST00000617938.4:c.*1182+60_*1182+61insTCTAAAGATAGAG	ENSP00000481158.1:n.*1182+60_*1182+61insTCTAAAGATAGAG
ENST00000621359.2:c.2210+60_2210+61insTCTAAAGATAGAG	ENSP00000481416.1:n.2210+60_2210+61insTCTAAAGATAGAG
NM_000251.2:c.2210+60_2210+61insTCTAAAGATAGAG , LRG_218t1:c.2210+60_2210+61insTCTAAAGATAGAG	NP_000242.1:n.2210+60_2210+61insTCTAAAGATAGAG
NM_001258281.1:c.2012+60_2012+61insTCTAAAGATAGAG	NP_001245210.1:n.2012+60_2012+61insTCTAAAGATAGAG
XM_005264332.2:c.2210+60_2210+61insTCTAAAGATAGAG	XP_005264389.2:n.2210+60_2210+61insTCTAAAGATAGAG
XM_011532867.1:c.2210+60_2210+61insTCTAAAGATAGAG	XP_011531169.1:n.2210+60_2210+61insTCTAAAGATAGAG
XR_939685.1:n.2282+60_2282+61insTCTAAAGATAGAG
XM_005264332.4:c.2210+60_2210+61insTCTAAAGATAGAG	XP_005264389.2:n.2210+60_2210+61insTCTAAAGATAGAG
XM_011532867.2:c.2210+60_2210+61insTCTAAAGATAGAG	XP_011531169.1:n.2210+60_2210+61insTCTAAAGATAGAG
XR_001738747.2:n.2272+60_2272+61insTCTAAAGATAGAG
XR_939685.2:n.2272+60_2272+61insTCTAAAGATAGAG
NM_000251.3:c.2210+60_2210+61insTCTAAAGATAGAG MANE Select	NP_000242.1:n.2210+60_2210+61insTCTAAAGATAGAG