Canonical Allele Identifier: CA2495872512

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475174_47475175delinsTC , CM000664.2:g.47475174_47475175delinsTC	GRCh38
NC_000002.11:g.47702313_47702314delinsTC , CM000664.1:g.47702313_47702314delinsTC	GRCh37
NC_000002.10:g.47555817_47555818delinsTC	NCBI36
NG_007110.2:g.77051_77052delinsTC , LRG_218:g.77051_77052delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.1909_1910delinsTC	ENSP00000495641.2:p.Ser637=
ENST00000233146.7:c.1909_1910delinsTC MANE Select	ENSP00000233146.2:p.Ser637=
ENST00000543555.6:c.1711_1712delinsTC	ENSP00000442697.1:p.Ser571=
ENST00000644092.1:c.*209_*210delinsTC	ENSP00000496351.1:n.*209_*210delinsTC
ENST00000645339.1:c.1909_1910delinsTC	ENSP00000496441.1:p.Ser637=
ENST00000645506.1:c.1909_1910delinsTC	ENSP00000495455.1:p.Ser637=
ENST00000646415.1:c.1909_1910delinsTC	ENSP00000495543.1:p.Ser637=
ENST00000233146.6:c.1909_1910delinsTC	ENSP00000233146.2:p.Ser637=
ENST00000406134.5:c.1909_1910delinsTC	ENSP00000384199.1:p.Ser637=
ENST00000543555.5:c.1711_1712delinsTC	ENSP00000442697.1:p.Ser571=
ENST00000610696.4:c.*305_*306delinsTC	ENSP00000483159.1:n.*305_*306delinsTC
ENST00000613514.4:c.*449_*450delinsTC	ENSP00000484137.1:n.*449_*450delinsTC
ENST00000617333.3:c.*675_*676delinsTC	ENSP00000482468.1:n.*675_*676delinsTC
ENST00000617938.4:c.*881_*882delinsTC	ENSP00000481158.1:n.*881_*882delinsTC
ENST00000621359.2:c.1909_1910delinsTC	ENSP00000481416.1:p.Ser637=
NM_000251.2:c.1909_1910delinsTC , LRG_218t1:c.1909_1910delinsTC	NP_000242.1:p.Ser637=
NM_001258281.1:c.1711_1712delinsTC	NP_001245210.1:p.Ser571=
XM_005264332.2:c.1909_1910delinsTC	XP_005264389.2:p.Ser637=
XM_011532867.1:c.1909_1910delinsTC	XP_011531169.1:p.Ser637=
XR_939685.1:n.1981_1982delinsTC
XM_005264332.4:c.1909_1910delinsTC	XP_005264389.2:p.Ser637=
XM_011532867.2:c.1909_1910delinsTC	XP_011531169.1:p.Ser637=
XR_001738747.2:n.1971_1972delinsTC
XR_939685.2:n.1971_1972delinsTC
NM_000251.3:c.1909_1910delinsTC MANE Select	NP_000242.1:p.Ser637=