Canonical Allele Identifier: CA2586964830

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475119del , CM000664.2:g.47475119del	GRCh38
NC_000002.11:g.47702258del , CM000664.1:g.47702258del	GRCh37
NC_000002.10:g.47555762del	NCBI36
NG_007110.2:g.76996del , LRG_218:g.76996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1854del	ENSP00000495641.2:p.Tyr619MetfsTer16
ENST00000233146.7:c.1854del MANE Select	ENSP00000233146.2:p.Tyr619MetfsTer16
ENST00000543555.6:c.1656del	ENSP00000442697.1:p.Tyr553MetfsTer16
ENST00000644092.1:c.*154del	ENSP00000496351.1:n.*154del
ENST00000645339.1:c.1854del	ENSP00000496441.1:p.Tyr619MetfsTer16
ENST00000645506.1:c.1854del	ENSP00000495455.1:p.Tyr619MetfsTer16
ENST00000646415.1:c.1854del	ENSP00000495543.1:p.Tyr619MetfsTer16
ENST00000233146.6:c.1854del	ENSP00000233146.2:p.Tyr619MetfsTer16
ENST00000406134.5:c.1854del	ENSP00000384199.1:p.Tyr619MetfsTer16
ENST00000543555.5:c.1656del	ENSP00000442697.1:p.Tyr553MetfsTer16
ENST00000610696.4:c.*250del	ENSP00000483159.1:n.*250del
ENST00000613514.4:c.*394del	ENSP00000484137.1:n.*394del
ENST00000617333.3:c.*620del	ENSP00000482468.1:n.*620del
ENST00000617938.4:c.*826del	ENSP00000481158.1:n.*826del
ENST00000621359.2:c.1854del	ENSP00000481416.1:p.Tyr619MetfsTer16
NM_000251.2:c.1854del , LRG_218t1:c.1854del	NP_000242.1:p.Tyr619MetfsTer16
NM_001258281.1:c.1656del	NP_001245210.1:p.Tyr553MetfsTer16
XM_005264332.2:c.1854del	XP_005264389.2:p.Tyr619MetfsTer16
XM_011532867.1:c.1854del	XP_011531169.1:p.Tyr619MetfsTer16
XR_939685.1:n.1926del
XM_005264332.4:c.1854del	XP_005264389.2:p.Tyr619MetfsTer16
XM_011532867.2:c.1854del	XP_011531169.1:p.Tyr619MetfsTer16
XR_001738747.2:n.1916del
XR_939685.2:n.1916del
NM_000251.3:c.1854del MANE Select	NP_000242.1:p.Tyr619MetfsTer16