Canonical Allele Identifier: CA2495877500

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47483126_47483127delinsGA , CM000664.2:g.47483126_47483127delinsGA	GRCh38
NC_000002.11:g.47710265_47710266delinsGA , CM000664.1:g.47710265_47710266delinsGA	GRCh37
NC_000002.10:g.47563769_47563770delinsGA	NCBI36
NG_007110.2:g.85003_85004delinsGA , LRG_218:g.85003_85004delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+2255_2634+2256delinsGA	ENSP00000495641.2:n.2634+2255_2634+2256delinsGA
ENST00000233146.7:c.*177_*178delinsGA MANE Select	ENSP00000233146.2:n.*177_*178delinsGA
ENST00000543555.6:c.*177_*178delinsGA	ENSP00000442697.1:n.*177_*178delinsGA
ENST00000644092.1:c.*934+2255_*934+2256delinsGA	ENSP00000496351.1:n.*934+2255_*934+2256delinsGA
ENST00000644900.1:c.487+2255_487+2256delinsGA
ENST00000645339.1:c.2634+2255_2634+2256delinsGA	ENSP00000496441.1:n.2634+2255_2634+2256delinsGA
ENST00000645506.1:c.2634+2255_2634+2256delinsGA	ENSP00000495455.1:n.2634+2255_2634+2256delinsGA
ENST00000646415.1:c.2634+2255_2634+2256delinsGA	ENSP00000495543.1:n.2634+2255_2634+2256delinsGA
ENST00000233146.6:c.*177_*178delinsGA	ENSP00000233146.2:n.*177_*178delinsGA
ENST00000406134.5:c.2634+2255_2634+2256delinsGA	ENSP00000384199.1:n.2634+2255_2634+2256delinsGA
ENST00000461394.5:n.75+2255_75+2256delinsGA
ENST00000543555.5:c.*177_*178delinsGA	ENSP00000442697.1:n.*177_*178delinsGA
NM_000251.2:c.*177_*178delinsGA , LRG_218t1:c.*177_*178delinsGA	NP_000242.1:n.*177_*178delinsGA
NM_001258281.1:c.*177_*178delinsGA	NP_001245210.1:n.*177_*178delinsGA
XM_005264332.2:c.2634+2255_2634+2256delinsGA	XP_005264389.2:n.2634+2255_2634+2256delinsGA
XM_011532867.1:c.2634+2255_2634+2256delinsGA	XP_011531169.1:n.2634+2255_2634+2256delinsGA
XR_939685.1:n.2706+2255_2706+2256delinsGA
XM_005264332.4:c.2634+2255_2634+2256delinsGA	XP_005264389.2:n.2634+2255_2634+2256delinsGA
XM_011532867.2:c.2634+2255_2634+2256delinsGA	XP_011531169.1:n.2634+2255_2634+2256delinsGA
XR_001738747.2:n.2696+2255_2696+2256delinsGA
XR_939685.2:n.2696+2255_2696+2256delinsGA
NM_000251.3:c.*177_*178delinsGA MANE Select	NP_000242.1:n.*177_*178delinsGA