Canonical Allele Identifier: CA769423824

Gene: MSH2

Linked Data

• dbSNP Id: rs1307462176
• MyVariant Identifiers: chr2:g.47693641_47693643del (hg19) ; chr2:g.47466502_47466504del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47466506_47466508del , CM000664.2:g.47466506_47466508del	GRCh38
NC_000002.11:g.47693645_47693647del , CM000664.1:g.47693645_47693647del	GRCh37
NC_000002.10:g.47547149_47547151del	NCBI36
NG_007110.2:g.68383_68385del , LRG_218:g.68383_68385del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.1511-152_1511-150del	ENSP00000495641.2:n.1511-152_1511-150del
ENST00000233146.7:c.1511-152_1511-150del MANE Select	ENSP00000233146.2:n.1511-152_1511-150del
ENST00000543555.6:c.1313-152_1313-150del	ENSP00000442697.1:n.1313-152_1313-150del
ENST00000644092.1:c.1511-152_1511-150del	ENSP00000496351.1:n.1511-152_1511-150del
ENST00000645339.1:c.1511-152_1511-150del	ENSP00000496441.1:n.1511-152_1511-150del
ENST00000645506.1:c.1511-152_1511-150del	ENSP00000495455.1:n.1511-152_1511-150del
ENST00000646415.1:c.1511-152_1511-150del	ENSP00000495543.1:n.1511-152_1511-150del
ENST00000233146.6:c.1511-152_1511-150del	ENSP00000233146.2:n.1511-152_1511-150del
ENST00000406134.5:c.1511-152_1511-150del	ENSP00000384199.1:n.1511-152_1511-150del
ENST00000543555.5:c.1313-152_1313-150del	ENSP00000442697.1:n.1313-152_1313-150del
ENST00000610696.4:c.1511-152_1511-150del	ENSP00000483159.1:n.1511-152_1511-150del
ENST00000613514.4:c.*51-152_*51-150del	ENSP00000484137.1:n.*51-152_*51-150del
ENST00000617333.3:c.*277-152_*277-150del	ENSP00000482468.1:n.*277-152_*277-150del
ENST00000617938.4:c.*483-152_*483-150del	ENSP00000481158.1:n.*483-152_*483-150del
ENST00000621359.2:c.1511-152_1511-150del	ENSP00000481416.1:n.1511-152_1511-150del
NM_000251.2:c.1511-152_1511-150del , LRG_218t1:c.1511-152_1511-150del	NP_000242.1:n.1511-152_1511-150del
NM_001258281.1:c.1313-152_1313-150del	NP_001245210.1:n.1313-152_1313-150del
XM_005264332.2:c.1511-152_1511-150del	XP_005264389.2:n.1511-152_1511-150del
XM_011532867.1:c.1511-152_1511-150del	XP_011531169.1:n.1511-152_1511-150del
XR_939685.1:n.1583-152_1583-150del
XM_005264332.4:c.1511-152_1511-150del	XP_005264389.2:n.1511-152_1511-150del
XM_011532867.2:c.1511-152_1511-150del	XP_011531169.1:n.1511-152_1511-150del
XR_001738747.2:n.1573-152_1573-150del
XR_939685.2:n.1573-152_1573-150del
NM_000251.3:c.1511-152_1511-150del MANE Select	NP_000242.1:n.1511-152_1511-150del