Canonical Allele Identifier: CA471816651

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565222G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766958G>T , CM000672.2:g.129766958G>T	GRCh38
NC_000010.10:g.131565222G>T , CM000672.1:g.131565222G>T	GRCh37
NC_000010.9:g.131455212G>T	NCBI36
NG_052673.1:g.304775G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.678G>T	ENSP00000302111.7:p.Ala226=
ENST00000651593.1:c.585G>T MANE Select	ENSP00000498729.1:p.Ala195=
ENST00000306010.7:c.678G>T	ENSP00000302111.7:p.Ala226=
NM_002412.3:c.678G>T	NP_002403.2:p.Ala226=
NM_002412.4:c.678G>T	NP_002403.2:p.Ala226=
XM_005252682.2:c.585G>T	XP_005252739.1:p.Ala195=
XM_006717863.2:c.408G>T	XP_006717926.1:p.Ala136=
XM_011539817.1:c.594G>T	XP_011538119.1:p.Ala198=
NM_002412.5:c.585G>T MANE Select	NP_002403.3:p.Ala195=
XM_017016275.1:c.408G>T	XP_016871764.1:p.Ala136=