Canonical Allele Identifier: CA2495867204

Gene: MSH2

Linked Data

• dbSNP Id: rs1666888608
• gnomAD v4: 2-47466602-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47466607del , CM000664.2:g.47466607del	GRCh38
NC_000002.11:g.47693746del , CM000664.1:g.47693746del	GRCh37
NC_000002.10:g.47547250del	NCBI36
NG_007110.2:g.68484del , LRG_218:g.68484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1511-51del	ENSP00000495641.2:n.1511-51del
ENST00000233146.7:c.1511-51del MANE Select	ENSP00000233146.2:n.1511-51del
ENST00000543555.6:c.1313-51del	ENSP00000442697.1:n.1313-51del
ENST00000644092.1:c.1511-51del	ENSP00000496351.1:n.1511-51del
ENST00000645339.1:c.1511-51del	ENSP00000496441.1:n.1511-51del
ENST00000645506.1:c.1511-51del	ENSP00000495455.1:n.1511-51del
ENST00000646415.1:c.1511-51del	ENSP00000495543.1:n.1511-51del
ENST00000233146.6:c.1511-51del	ENSP00000233146.2:n.1511-51del
ENST00000406134.5:c.1511-51del	ENSP00000384199.1:n.1511-51del
ENST00000543555.5:c.1313-51del	ENSP00000442697.1:n.1313-51del
ENST00000610696.4:c.1511-51del	ENSP00000483159.1:n.1511-51del
ENST00000613514.4:c.*51-51del	ENSP00000484137.1:n.*51-51del
ENST00000617333.3:c.*277-51del	ENSP00000482468.1:n.*277-51del
ENST00000617938.4:c.*483-51del	ENSP00000481158.1:n.*483-51del
ENST00000621359.2:c.1511-51del	ENSP00000481416.1:n.1511-51del
NM_000251.2:c.1511-51del , LRG_218t1:c.1511-51del	NP_000242.1:n.1511-51del
NM_001258281.1:c.1313-51del	NP_001245210.1:n.1313-51del
XM_005264332.2:c.1511-51del	XP_005264389.2:n.1511-51del
XM_011532867.1:c.1511-51del	XP_011531169.1:n.1511-51del
XR_939685.1:n.1583-51del
XM_005264332.4:c.1511-51del	XP_005264389.2:n.1511-51del
XM_011532867.2:c.1511-51del	XP_011531169.1:n.1511-51del
XR_001738747.2:n.1573-51del
XR_939685.2:n.1573-51del
NM_000251.3:c.1511-51del MANE Select	NP_000242.1:n.1511-51del