Canonical Allele Identifier: CA2495872565

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475232_47475233delinsAC , CM000664.2:g.47475232_47475233delinsAC	GRCh38
NC_000002.11:g.47702371_47702372delinsAC , CM000664.1:g.47702371_47702372delinsAC	GRCh37
NC_000002.10:g.47555875_47555876delinsAC	NCBI36
NG_007110.2:g.77109_77110delinsAC , LRG_218:g.77109_77110delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1967_1968delinsAC	ENSP00000495641.2:p.Tyr656=
ENST00000233146.7:c.1967_1968delinsAC MANE Select	ENSP00000233146.2:p.Tyr656=
ENST00000543555.6:c.1769_1770delinsAC	ENSP00000442697.1:p.Tyr590=
ENST00000644092.1:c.*267_*268delinsAC	ENSP00000496351.1:n.*267_*268delinsAC
ENST00000645339.1:c.1967_1968delinsAC	ENSP00000496441.1:p.Tyr656=
ENST00000645506.1:c.1967_1968delinsAC	ENSP00000495455.1:p.Tyr656=
ENST00000646415.1:c.1967_1968delinsAC	ENSP00000495543.1:p.Tyr656=
ENST00000233146.6:c.1967_1968delinsAC	ENSP00000233146.2:p.Tyr656=
ENST00000406134.5:c.1967_1968delinsAC	ENSP00000384199.1:p.Tyr656=
ENST00000543555.5:c.1769_1770delinsAC	ENSP00000442697.1:p.Tyr590=
ENST00000610696.4:c.*363_*364delinsAC	ENSP00000483159.1:n.*363_*364delinsAC
ENST00000613514.4:c.*507_*508delinsAC	ENSP00000484137.1:n.*507_*508delinsAC
ENST00000617333.3:c.*733_*734delinsAC	ENSP00000482468.1:n.*733_*734delinsAC
ENST00000617938.4:c.*939_*940delinsAC	ENSP00000481158.1:n.*939_*940delinsAC
ENST00000621359.2:c.1967_1968delinsAC	ENSP00000481416.1:p.Tyr656=
NM_000251.2:c.1967_1968delinsAC , LRG_218t1:c.1967_1968delinsAC	NP_000242.1:p.Tyr656=
NM_001258281.1:c.1769_1770delinsAC	NP_001245210.1:p.Tyr590=
XM_005264332.2:c.1967_1968delinsAC	XP_005264389.2:p.Tyr656=
XM_011532867.1:c.1967_1968delinsAC	XP_011531169.1:p.Tyr656=
XR_939685.1:n.2039_2040delinsAC
XM_005264332.4:c.1967_1968delinsAC	XP_005264389.2:p.Tyr656=
XM_011532867.2:c.1967_1968delinsAC	XP_011531169.1:p.Tyr656=
XR_001738747.2:n.2029_2030delinsAC
XR_939685.2:n.2029_2030delinsAC
NM_000251.3:c.1967_1968delinsAC MANE Select	NP_000242.1:p.Tyr656=