Canonical Allele Identifier: CA2580067344

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1777666
• ClinVar RCV Id: RCV002405837

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403358_47403376del , CM000664.2:g.47403358_47403376del	GRCh38
NC_000002.11:g.47630497_47630515del , CM000664.1:g.47630497_47630515del	GRCh37
NC_000002.10:g.47484001_47484019del	NCBI36
NG_007110.2:g.5235_5253del , LRG_218:g.5235_5253del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.167_185del	ENSP00000495641.2:p.Glu56GlyfsTer2
ENST00000233146.7:c.167_185del MANE Select	ENSP00000233146.2:p.Glu56GlyfsTer2
ENST00000543555.6:c.-30-2_-14del
ENST00000644092.1:c.167_185del	ENSP00000496351.1:p.Glu56GlyfsTer2
ENST00000645339.1:c.167_185del	ENSP00000496441.1:p.Glu56GlyfsTer2
ENST00000645506.1:c.167_185del	ENSP00000495455.1:p.Glu56GlyfsTer2
ENST00000646415.1:c.167_185del	ENSP00000495543.1:p.Glu56GlyfsTer2
ENST00000233146.6:c.167_185del	ENSP00000233146.2:p.Glu56GlyfsTer2
ENST00000406134.5:c.167_185del	ENSP00000384199.1:p.Glu56GlyfsTer2
ENST00000454849.5:c.-30-2_-14del
ENST00000543555.5:c.-30-2_-14del
ENST00000610696.4:c.167_185del	ENSP00000483159.1:p.Glu56GlyfsTer2
ENST00000613514.4:c.167_185del	ENSP00000484137.1:p.Glu56GlyfsTer2
ENST00000617333.3:c.167_185del	ENSP00000482468.1:p.Glu56GlyfsTer2
ENST00000617938.4:c.167_185del	ENSP00000481158.1:p.Glu56GlyfsTer2
ENST00000621359.2:c.167_185del	ENSP00000481416.1:p.Glu56GlyfsTer2
NM_000251.2:c.167_185del , LRG_218t1:c.167_185del	NP_000242.1:p.Glu56GlyfsTer2
NM_001258281.1:c.-30-2_-14del
XM_005264332.2:c.167_185del	XP_005264389.2:p.Glu56GlyfsTer2
XM_011532867.1:c.167_185del	XP_011531169.1:p.Glu56GlyfsTer2
XR_939685.1:n.239_257del
XM_005264332.4:c.167_185del	XP_005264389.2:p.Glu56GlyfsTer2
XM_011532867.2:c.167_185del	XP_011531169.1:p.Glu56GlyfsTer2
XR_001738747.2:n.229_247del
XR_939685.2:n.229_247del
NM_000251.3:c.167_185del MANE Select	NP_000242.1:p.Glu56GlyfsTer2