Canonical Allele Identifier: CA2576960908

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47414416_47414422del , CM000664.2:g.47414416_47414422del	GRCh38
NC_000002.11:g.47641555_47641561del , CM000664.1:g.47641555_47641561del	GRCh37
NC_000002.10:g.47495059_47495065del	NCBI36
NG_007110.2:g.16293_16299del , LRG_218:g.16293_16299del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.940_942+4del
ENST00000233146.7:c.940_942+4del
ENST00000543555.6:c.742_744+4del
ENST00000644092.1:c.940_942+4del
ENST00000645339.1:c.940_942+4del
ENST00000645506.1:c.940_942+4del
ENST00000646415.1:c.940_942+4del
ENST00000233146.6:c.940_942+4del
ENST00000406134.5:c.940_942+4del
ENST00000543555.5:c.742_744+4del
ENST00000610696.4:c.940_942+4del
ENST00000613514.4:c.940_942+4del
ENST00000617333.3:c.940_942+4del
ENST00000617938.4:c.940_942+4del
ENST00000621359.2:c.940_942+4del
NM_000251.2:c.940_942+4del , LRG_218t1:c.940_942+4del
NM_001258281.1:c.742_744+4del
XM_005264332.2:c.940_942+4del
XM_011532867.1:c.940_942+4del
XR_939685.1:n.1012_1014+4del
XM_005264332.4:c.940_942+4del
XM_011532867.2:c.940_942+4del
XR_001738747.2:n.1002_1004+4del
XR_939685.2:n.1002_1004+4del
NM_000251.3:c.940_942+4del