Canonical Allele Identifier: CA2586969177

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47462972_47463202del , CM000664.2:g.47462972_47463202del	GRCh38
NC_000002.11:g.47690111_47690341del , CM000664.1:g.47690111_47690341del	GRCh37
NC_000002.10:g.47543615_47543845del	NCBI36
NG_007110.2:g.64849_65079del , LRG_218:g.64849_65079del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644900.2:c.1387-59_1510+48del
ENST00000233146.7:c.1387-59_1510+48del
ENST00000543555.6:c.1189-59_1312+48del
ENST00000644092.1:c.1387-59_1510+48del
ENST00000645339.1:c.1387-59_1510+48del
ENST00000645506.1:c.1387-59_1510+48del
ENST00000646415.1:c.1387-59_1510+48del
ENST00000233146.6:c.1387-59_1510+48del
ENST00000406134.5:c.1387-59_1510+48del
ENST00000543555.5:c.1189-59_1312+48del
ENST00000610696.4:c.1387-59_1510+48del
ENST00000613514.4:c.1387-59_*50+48del
ENST00000617333.3:c.*153-59_*276+48del
ENST00000617938.4:c.*359-59_*482+48del
ENST00000621359.2:c.1387-59_1510+48del
NM_000251.2:c.1387-59_1510+48del , LRG_218t1:c.1387-59_1510+48del
NM_001258281.1:c.1189-59_1312+48del
XM_005264332.2:c.1387-59_1510+48del
XM_011532867.1:c.1387-59_1510+48del
XR_939685.1:n.1459-59_1582+48del
XM_005264332.4:c.1387-59_1510+48del
XM_011532867.2:c.1387-59_1510+48del
XR_001738747.2:n.1449-59_1572+48del
XR_939685.2:n.1449-59_1572+48del
NM_000251.3:c.1387-59_1510+48del