Canonical Allele Identifier: CA2831039091

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403145_47403154del , CM000664.2:g.47403145_47403154del	GRCh38
NC_000002.11:g.47630284_47630293del , CM000664.1:g.47630284_47630293del	GRCh37
NC_000002.10:g.47483788_47483797del	NCBI36
NG_007110.2:g.5022_5031del , LRG_218:g.5022_5031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-61_-52del	ENSP00000442697.1:n.-61_-52del
ENST00000644092.1:c.-47_-38del	ENSP00000496351.1:n.-47_-38del
ENST00000645339.1:c.-47_-38del	ENSP00000496441.1:n.-47_-38del
ENST00000645506.1:c.-47_-38del	ENSP00000495455.1:n.-47_-38del
ENST00000646415.1:c.-47_-38del	ENSP00000495543.1:n.-47_-38del
ENST00000233146.6:c.-47_-38del	ENSP00000233146.2:n.-47_-38del
ENST00000406134.5:c.-47_-38del	ENSP00000384199.1:n.-47_-38del
ENST00000454849.5:c.-61_-52del	ENSP00000411482.1:n.-61_-52del
ENST00000543555.5:c.-61_-52del	ENSP00000442697.1:n.-61_-52del
NM_000251.2:c.-47_-38del , LRG_218t1:c.-47_-38del	NP_000242.1:n.-47_-38del
NM_001258281.1:c.-61_-52del	NP_001245210.1:n.-61_-52del
XM_005264332.2:c.-47_-38del	XP_005264389.2:n.-47_-38del
XM_011532867.1:c.-47_-38del	XP_011531169.1:n.-47_-38del
XR_939685.1:n.26_35del
XM_005264332.4:c.-47_-38del	XP_005264389.2:n.-47_-38del
XM_011532867.2:c.-47_-38del	XP_011531169.1:n.-47_-38del
XR_001738747.2:n.16_25del
XR_939685.2:n.16_25del