Canonical Allele Identifier: CA2495831034

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47409962_47409971delinsACTTCATCTC , CM000664.2:g.47409962_47409971delinsACTTCATCTC	GRCh38
NC_000002.11:g.47637101_47637110delinsACTTCATCTC , CM000664.1:g.47637101_47637110delinsACTTCATCTC	GRCh37
NC_000002.10:g.47490605_47490614delinsACTTCATCTC	NCBI36
NG_007110.2:g.11839_11848delinsACTTCATCTC , LRG_218:g.11839_11848delinsACTTCATCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.367-132_367-123delinsACTTCATCTC	ENSP00000495641.2:n.367-132_367-123delinsACTTCATCTC
ENST00000233146.7:c.367-132_367-123delinsACTTCATCTC MANE Select	ENSP00000233146.2:n.367-132_367-123delinsACTTCATCTC
ENST00000543555.6:c.169-132_169-123delinsACTTCATCTC	ENSP00000442697.1:n.169-132_169-123delinsACTTCATCTC
ENST00000644092.1:c.367-132_367-123delinsACTTCATCTC	ENSP00000496351.1:n.367-132_367-123delinsACTTCATCTC
ENST00000645339.1:c.367-132_367-123delinsACTTCATCTC	ENSP00000496441.1:n.367-132_367-123delinsACTTCATCTC
ENST00000645506.1:c.367-132_367-123delinsACTTCATCTC	ENSP00000495455.1:n.367-132_367-123delinsACTTCATCTC
ENST00000646415.1:c.367-132_367-123delinsACTTCATCTC	ENSP00000495543.1:n.367-132_367-123delinsACTTCATCTC
ENST00000233146.6:c.367-132_367-123delinsACTTCATCTC	ENSP00000233146.2:n.367-132_367-123delinsACTTCATCTC
ENST00000406134.5:c.367-132_367-123delinsACTTCATCTC	ENSP00000384199.1:n.367-132_367-123delinsACTTCATCTC
ENST00000454849.5:c.169-132_169-123delinsACTTCATCTC	ENSP00000411482.1:n.169-132_169-123delinsACTTCATCTC
ENST00000543555.5:c.169-132_169-123delinsACTTCATCTC	ENSP00000442697.1:n.169-132_169-123delinsACTTCATCTC
ENST00000610696.4:c.367-132_367-123delinsACTTCATCTC	ENSP00000483159.1:n.367-132_367-123delinsACTTCATCTC
ENST00000613514.4:c.367-132_367-123delinsACTTCATCTC	ENSP00000484137.1:n.367-132_367-123delinsACTTCATCTC
ENST00000617333.3:c.367-132_367-123delinsACTTCATCTC	ENSP00000482468.1:n.367-132_367-123delinsACTTCATCTC
ENST00000617938.4:c.367-132_367-123delinsACTTCATCTC	ENSP00000481158.1:n.367-132_367-123delinsACTTCATCTC
ENST00000621359.2:c.367-132_367-123delinsACTTCATCTC	ENSP00000481416.1:n.367-132_367-123delinsACTTCATCTC
NM_000251.2:c.367-132_367-123delinsACTTCATCTC , LRG_218t1:c.367-132_367-123delinsACTTCATCTC	NP_000242.1:n.367-132_367-123delinsACTTCATCTC
NM_001258281.1:c.169-132_169-123delinsACTTCATCTC	NP_001245210.1:n.169-132_169-123delinsACTTCATCTC
XM_005264332.2:c.367-132_367-123delinsACTTCATCTC	XP_005264389.2:n.367-132_367-123delinsACTTCATCTC
XM_011532867.1:c.367-132_367-123delinsACTTCATCTC	XP_011531169.1:n.367-132_367-123delinsACTTCATCTC
XR_939685.1:n.439-132_439-123delinsACTTCATCTC
XM_005264332.4:c.367-132_367-123delinsACTTCATCTC	XP_005264389.2:n.367-132_367-123delinsACTTCATCTC
XM_011532867.2:c.367-132_367-123delinsACTTCATCTC	XP_011531169.1:n.367-132_367-123delinsACTTCATCTC
XR_001738747.2:n.429-132_429-123delinsACTTCATCTC
XR_939685.2:n.429-132_429-123delinsACTTCATCTC
NM_000251.3:c.367-132_367-123delinsACTTCATCTC MANE Select	NP_000242.1:n.367-132_367-123delinsACTTCATCTC