Canonical Allele Identifier: CA471816683

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565246T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766982T>G , CM000672.2:g.129766982T>G	GRCh38
NC_000010.10:g.131565246T>G , CM000672.1:g.131565246T>G	GRCh37
NC_000010.9:g.131455236T>G	NCBI36
NG_052673.1:g.304799T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.702T>G	ENSP00000302111.7:p.Pro234=
ENST00000651593.1:c.609T>G MANE Select	ENSP00000498729.1:p.Pro203=
ENST00000306010.7:c.702T>G	ENSP00000302111.7:p.Pro234=
NM_002412.3:c.702T>G	NP_002403.2:p.Pro234=
NM_002412.4:c.702T>G	NP_002403.2:p.Pro234=
XM_005252682.2:c.609T>G	XP_005252739.1:p.Pro203=
XM_006717863.2:c.432T>G	XP_006717926.1:p.Pro144=
XM_011539817.1:c.618T>G	XP_011538119.1:p.Pro206=
NM_002412.5:c.609T>G MANE Select	NP_002403.3:p.Pro203=
XM_017016275.1:c.432T>G	XP_016871764.1:p.Pro144=