Canonical Allele Identifier: CA471816592

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565168G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766904G>T , CM000672.2:g.129766904G>T	GRCh38
NC_000010.10:g.131565168G>T , CM000672.1:g.131565168G>T	GRCh37
NC_000010.9:g.131455158G>T	NCBI36
NG_052673.1:g.304721G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.624G>T	ENSP00000302111.7:p.Gly208=
ENST00000651593.1:c.531G>T MANE Select	ENSP00000498729.1:p.Gly177=
ENST00000306010.7:c.624G>T	ENSP00000302111.7:p.Gly208=
NM_002412.3:c.624G>T	NP_002403.2:p.Gly208=
NM_002412.4:c.624G>T	NP_002403.2:p.Gly208=
XM_005252682.2:c.531G>T	XP_005252739.1:p.Gly177=
XM_006717863.2:c.354G>T	XP_006717926.1:p.Gly118=
XM_011539817.1:c.540G>T	XP_011538119.1:p.Gly180=
NM_002412.5:c.531G>T MANE Select	NP_002403.3:p.Gly177=
XM_017016275.1:c.354G>T	XP_016871764.1:p.Gly118=