Canonical Allele Identifier: CA021243

Gene: MSH2

Linked Data

• ClinVar Variation Id: 91116
• ClinVar RCV Id: RCV000076620
• dbSNP Id: rs63751013
• MyVariant Identifiers: chr2:g.47637372_47637375del (hg19) ; chr2:g.47410233_47410236del (hg38)
• PubMed: PMID:10404063

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47410233_47410236del , CM000664.2:g.47410233_47410236del	GRCh38
NC_000002.11:g.47637372_47637375del , CM000664.1:g.47637372_47637375del	GRCh37
NC_000002.10:g.47490876_47490879del	NCBI36
NG_007110.2:g.12110_12113del , LRG_218:g.12110_12113del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.506_509del	ENSP00000495641.2:p.Ile169ArgfsTer4
ENST00000233146.7:c.506_509del MANE Select	ENSP00000233146.2:p.Ile169ArgfsTer4
ENST00000543555.6:c.308_311del	ENSP00000442697.1:p.Ile103ArgfsTer4
ENST00000644092.1:c.506_509del	ENSP00000496351.1:p.Ile169ArgfsTer4
ENST00000645339.1:c.506_509del	ENSP00000496441.1:p.Ile169ArgfsTer4
ENST00000645506.1:c.506_509del	ENSP00000495455.1:p.Ile169ArgfsTer4
ENST00000646415.1:c.506_509del	ENSP00000495543.1:p.Ile169ArgfsTer4
ENST00000233146.6:c.506_509del	ENSP00000233146.2:p.Ile169ArgfsTer4
ENST00000406134.5:c.506_509del	ENSP00000384199.1:p.Ile169ArgfsTer4
ENST00000454849.5:c.308_311del	ENSP00000411482.1:p.Ile103ArgfsTer4
ENST00000543555.5:c.308_311del	ENSP00000442697.1:p.Ile103ArgfsTer4
ENST00000610696.4:c.506_509del	ENSP00000483159.1:p.Ile169ArgfsTer4
ENST00000613514.4:c.506_509del	ENSP00000484137.1:p.Ile169ArgfsTer4
ENST00000617333.3:c.506_509del	ENSP00000482468.1:p.Ile169ArgfsTer4
ENST00000617938.4:c.506_509del	ENSP00000481158.1:p.Ile169ArgfsTer4
ENST00000621359.2:c.506_509del	ENSP00000481416.1:p.Ile169ArgfsTer4
NM_000251.2:c.506_509del , LRG_218t1:c.506_509del	NP_000242.1:p.Ile169ArgfsTer4
NM_001258281.1:c.308_311del	NP_001245210.1:p.Ile103ArgfsTer4
XM_005264332.2:c.506_509del	XP_005264389.2:p.Ile169ArgfsTer4
XM_011532867.1:c.506_509del	XP_011531169.1:p.Ile169ArgfsTer4
XR_939685.1:n.578_581del
XM_005264332.4:c.506_509del	XP_005264389.2:p.Ile169ArgfsTer4
XM_011532867.2:c.506_509del	XP_011531169.1:p.Ile169ArgfsTer4
XR_001738747.2:n.568_571del
XR_939685.2:n.568_571del
NM_000251.3:c.506_509del MANE Select	NP_000242.1:p.Ile169ArgfsTer4