Canonical Allele Identifier: CA2580061388

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475026_47478520del , CM000664.2:g.47475026_47478520del	GRCh38
NC_000002.11:g.47702165_47705659del , CM000664.1:g.47702165_47705659del	GRCh37
NC_000002.10:g.47555669_47559163del	NCBI36
NG_007110.2:g.76903_80397del , LRG_218:g.76903_80397del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1761_2458+1del
ENST00000233146.7:c.1761_2458+1del
ENST00000543555.6:c.1563_2260+1del
ENST00000644092.1:c.*61_*758+1del
ENST00000645339.1:c.1761_2458+1del
ENST00000645506.1:c.1761_2458+1del
ENST00000646415.1:c.1761_2458+1del
ENST00000233146.6:c.1761_2458+1del
ENST00000406134.5:c.1761_2458+1del
ENST00000543555.5:c.1563_2260+1del
ENST00000610696.4:c.*157_*854+1del
ENST00000613514.4:c.*301_*998+1del
ENST00000617333.3:c.*527_*1224+1del
ENST00000617938.4:c.*733_*1430+1del
ENST00000621359.2:c.1761_*24+1del
NM_000251.2:c.1761_2458+1del , LRG_218t1:c.1761_2458+1del
NM_001258281.1:c.1563_2260+1del
XM_005264332.2:c.1761_2458+1del
XM_011532867.1:c.1761_2458+1del
XR_939685.1:n.1833_2530+1del
XM_005264332.4:c.1761_2458+1del
XM_011532867.2:c.1761_2458+1del
XR_001738747.2:n.1823_2520+1del
XR_939685.2:n.1823_2520+1del
NM_000251.3:c.1761_2458+1del