Canonical Allele Identifier: CA022028

Gene: MSH2

Linked Data

• ClinVar Variation Id: 91179
• ClinVar RCV Id: RCV000076683
• dbSNP Id: rs587779174
• MyVariant Identifiers: chr2:g.47639598del (hg19) ; chr2:g.47412459del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47412459del , CM000664.2:g.47412459del	GRCh38
NC_000002.11:g.47639598del , CM000664.1:g.47639598del	GRCh37
NC_000002.10:g.47493102del	NCBI36
NG_007110.2:g.14336del , LRG_218:g.14336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.691del	ENSP00000495641.2:p.Asp231ThrfsTer15
ENST00000233146.7:c.691del MANE Select	ENSP00000233146.2:p.Asp231ThrfsTer15
ENST00000543555.6:c.493del	ENSP00000442697.1:p.Asp165ThrfsTer15
ENST00000644092.1:c.691del	ENSP00000496351.1:p.Asp231ThrfsTer15
ENST00000645339.1:c.691del	ENSP00000496441.1:p.Asp231ThrfsTer15
ENST00000645506.1:c.691del	ENSP00000495455.1:p.Asp231ThrfsTer15
ENST00000646415.1:c.691del	ENSP00000495543.1:p.Asp231ThrfsTer15
ENST00000233146.6:c.691del	ENSP00000233146.2:p.Asp231ThrfsTer15
ENST00000406134.5:c.691del	ENSP00000384199.1:p.Asp231ThrfsTer15
ENST00000543555.5:c.493del	ENSP00000442697.1:p.Asp165ThrfsTer15
ENST00000610696.4:c.691del	ENSP00000483159.1:p.Asp231ThrfsTer15
ENST00000613514.4:c.691del	ENSP00000484137.1:p.Asp231ThrfsTer15
ENST00000617333.3:c.691del	ENSP00000482468.1:p.Asp231ThrfsTer15
ENST00000617938.4:c.691del	ENSP00000481158.1:p.Asp231ThrfsTer15
ENST00000621359.2:c.691del	ENSP00000481416.1:p.Asp231ThrfsTer15
NM_000251.2:c.691del , LRG_218t1:c.691del	NP_000242.1:p.Asp231ThrfsTer15
NM_001258281.1:c.493del	NP_001245210.1:p.Asp165ThrfsTer15
XM_005264332.2:c.691del	XP_005264389.2:p.Asp231ThrfsTer15
XM_011532867.1:c.691del	XP_011531169.1:p.Asp231ThrfsTer15
XR_939685.1:n.763del
XM_005264332.4:c.691del	XP_005264389.2:p.Asp231ThrfsTer15
XM_011532867.2:c.691del	XP_011531169.1:p.Asp231ThrfsTer15
XR_001738747.2:n.753del
XR_939685.2:n.753del
NM_000251.3:c.691del MANE Select	NP_000242.1:p.Asp231ThrfsTer15