Canonical Allele Identifier: CA658655658

Gene: MSH2

Linked Data

• ClinVar Variation Id: 455473
• ClinVar RCV Id: RCV000535946
• dbSNP Id: rs1553348794
• MyVariant Identifiers: chr2:g.47630445del (hg19) ; chr2:g.47403306del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403306del , CM000664.2:g.47403306del	GRCh38
NC_000002.11:g.47630445del , CM000664.1:g.47630445del	GRCh37
NC_000002.10:g.47483949del	NCBI36
NG_007110.2:g.5183del , LRG_218:g.5183del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.115del	ENSP00000495641.2:p.Arg39GlyfsTer25
ENST00000233146.7:c.115del MANE Select	ENSP00000233146.2:p.Arg39GlyfsTer25
ENST00000543555.6:c.-30-54del	ENSP00000442697.1:n.-30-54del
ENST00000644092.1:c.115del	ENSP00000496351.1:p.Arg39GlyfsTer25
ENST00000645339.1:c.115del	ENSP00000496441.1:p.Arg39GlyfsTer25
ENST00000645506.1:c.115del	ENSP00000495455.1:p.Arg39GlyfsTer25
ENST00000646415.1:c.115del	ENSP00000495543.1:p.Arg39GlyfsTer25
ENST00000233146.6:c.115del	ENSP00000233146.2:p.Arg39GlyfsTer25
ENST00000406134.5:c.115del	ENSP00000384199.1:p.Arg39GlyfsTer25
ENST00000454849.5:c.-30-54del	ENSP00000411482.1:n.-30-54del
ENST00000543555.5:c.-30-54del	ENSP00000442697.1:n.-30-54del
ENST00000610696.4:c.115del	ENSP00000483159.1:p.Arg39GlyfsTer25
ENST00000613514.4:c.115del	ENSP00000484137.1:p.Arg39GlyfsTer25
ENST00000617333.3:c.115del	ENSP00000482468.1:p.Arg39GlyfsTer25
ENST00000617938.4:c.115del	ENSP00000481158.1:p.Arg39GlyfsTer25
ENST00000621359.2:c.115del	ENSP00000481416.1:p.Arg39GlyfsTer25
NM_000251.2:c.115del , LRG_218t1:c.115del	NP_000242.1:p.Arg39GlyfsTer25
NM_001258281.1:c.-30-54del	NP_001245210.1:n.-30-54del
XM_005264332.2:c.115del	XP_005264389.2:p.Arg39GlyfsTer25
XM_011532867.1:c.115del	XP_011531169.1:p.Arg39GlyfsTer25
XR_939685.1:n.187del
XM_005264332.4:c.115del	XP_005264389.2:p.Arg39GlyfsTer25
XM_011532867.2:c.115del	XP_011531169.1:p.Arg39GlyfsTer25
XR_001738747.2:n.177del
XR_939685.2:n.177del
NM_000251.3:c.115del MANE Select	NP_000242.1:p.Arg39GlyfsTer25