Canonical Allele Identifier: CA891842879

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403297_47407172del , CM000664.2:g.47403297_47407172del	GRCh38
NC_000002.11:g.47630436_47634311del , CM000664.1:g.47630436_47634311del	GRCh37
NC_000002.10:g.47483940_47487815del	NCBI36
NG_007110.2:g.5174_9049del , LRG_218:g.5174_9049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.106_212-1229del
ENST00000233146.7:c.106_212-1229del
ENST00000543555.6:c.-30-63_14-1229del
ENST00000644092.1:c.106_212-1229del
ENST00000645339.1:c.106_212-1229del
ENST00000645506.1:c.106_212-1229del
ENST00000646415.1:c.106_212-1229del
ENST00000233146.6:c.106_212-1229del
ENST00000406134.5:c.106_212-1229del
ENST00000454849.5:c.-30-63_14-1229del
ENST00000543555.5:c.-30-63_14-1229del
ENST00000610696.4:c.106_212-1229del
ENST00000613514.4:c.106_212-1229del
ENST00000617333.3:c.106_212-1229del
ENST00000617938.4:c.106_212-1229del
ENST00000621359.2:c.106_212-1229del
NM_000251.2:c.106_212-1229del , LRG_218t1:c.106_212-1229del
NM_001258281.1:c.-30-63_14-1229del
XM_005264332.2:c.106_212-1229del
XM_011532867.1:c.106_212-1229del
XR_939685.1:n.178_284-1229del
XM_005264332.4:c.106_212-1229del
XM_011532867.2:c.106_212-1229del
XR_001738747.2:n.168_274-1229del
XR_939685.2:n.168_274-1229del
NM_000251.3:c.106_212-1229del