Canonical Allele Identifier: CA2495872568

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475233_47475234delinsCT , CM000664.2:g.47475233_47475234delinsCT	GRCh38
NC_000002.11:g.47702372_47702373delinsCT , CM000664.1:g.47702372_47702373delinsCT	GRCh37
NC_000002.10:g.47555876_47555877delinsCT	NCBI36
NG_007110.2:g.77110_77111delinsCT , LRG_218:g.77110_77111delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1968_1969delinsCT	ENSP00000495641.2:p.Tyr656=
ENST00000233146.7:c.1968_1969delinsCT MANE Select	ENSP00000233146.2:p.Tyr656=
ENST00000543555.6:c.1770_1771delinsCT	ENSP00000442697.1:p.Tyr590=
ENST00000644092.1:c.*268_*269delinsCT	ENSP00000496351.1:n.*268_*269delinsCT
ENST00000645339.1:c.1968_1969delinsCT	ENSP00000496441.1:p.Tyr656=
ENST00000645506.1:c.1968_1969delinsCT	ENSP00000495455.1:p.Tyr656=
ENST00000646415.1:c.1968_1969delinsCT	ENSP00000495543.1:p.Tyr656=
ENST00000233146.6:c.1968_1969delinsCT	ENSP00000233146.2:p.Tyr656=
ENST00000406134.5:c.1968_1969delinsCT	ENSP00000384199.1:p.Tyr656=
ENST00000543555.5:c.1770_1771delinsCT	ENSP00000442697.1:p.Tyr590=
ENST00000610696.4:c.*364_*365delinsCT	ENSP00000483159.1:n.*364_*365delinsCT
ENST00000613514.4:c.*508_*509delinsCT	ENSP00000484137.1:n.*508_*509delinsCT
ENST00000617333.3:c.*734_*735delinsCT	ENSP00000482468.1:n.*734_*735delinsCT
ENST00000617938.4:c.*940_*941delinsCT	ENSP00000481158.1:n.*940_*941delinsCT
ENST00000621359.2:c.1968_1969delinsCT	ENSP00000481416.1:p.Tyr656=
NM_000251.2:c.1968_1969delinsCT , LRG_218t1:c.1968_1969delinsCT	NP_000242.1:p.Tyr656=
NM_001258281.1:c.1770_1771delinsCT	NP_001245210.1:p.Tyr590=
XM_005264332.2:c.1968_1969delinsCT	XP_005264389.2:p.Tyr656=
XM_011532867.1:c.1968_1969delinsCT	XP_011531169.1:p.Tyr656=
XR_939685.1:n.2040_2041delinsCT
XM_005264332.4:c.1968_1969delinsCT	XP_005264389.2:p.Tyr656=
XM_011532867.2:c.1968_1969delinsCT	XP_011531169.1:p.Tyr656=
XR_001738747.2:n.2030_2031delinsCT
XR_939685.2:n.2030_2031delinsCT
NM_000251.3:c.1968_1969delinsCT MANE Select	NP_000242.1:p.Tyr656=