Canonical Allele Identifier: CA471816655

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565225A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766961A>T , CM000672.2:g.129766961A>T	GRCh38
NC_000010.10:g.131565225A>T , CM000672.1:g.131565225A>T	GRCh37
NC_000010.9:g.131455215A>T	NCBI36
NG_052673.1:g.304778A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.681A>T	ENSP00000302111.7:p.Gly227=
ENST00000651593.1:c.588A>T MANE Select	ENSP00000498729.1:p.Gly196=
ENST00000306010.7:c.681A>T	ENSP00000302111.7:p.Gly227=
NM_002412.3:c.681A>T	NP_002403.2:p.Gly227=
NM_002412.4:c.681A>T	NP_002403.2:p.Gly227=
XM_005252682.2:c.588A>T	XP_005252739.1:p.Gly196=
XM_006717863.2:c.411A>T	XP_006717926.1:p.Gly137=
XM_011539817.1:c.597A>T	XP_011538119.1:p.Gly199=
NM_002412.5:c.588A>T MANE Select	NP_002403.3:p.Gly196=
XM_017016275.1:c.411A>T	XP_016871764.1:p.Gly137=