Canonical Allele Identifier: CA471816668

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565237C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766973C>T , CM000672.2:g.129766973C>T	GRCh38
NC_000010.10:g.131565237C>T , CM000672.1:g.131565237C>T	GRCh37
NC_000010.9:g.131455227C>T	NCBI36
NG_052673.1:g.304790C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.693C>T	ENSP00000302111.7:p.Gly231=
ENST00000651593.1:c.600C>T MANE Select	ENSP00000498729.1:p.Gly200=
ENST00000306010.7:c.693C>T	ENSP00000302111.7:p.Gly231=
NM_002412.3:c.693C>T	NP_002403.2:p.Gly231=
NM_002412.4:c.693C>T	NP_002403.2:p.Gly231=
XM_005252682.2:c.600C>T	XP_005252739.1:p.Gly200=
XM_006717863.2:c.423C>T	XP_006717926.1:p.Gly141=
XM_011539817.1:c.609C>T	XP_011538119.1:p.Gly203=
NM_002412.5:c.600C>T MANE Select	NP_002403.3:p.Gly200=
XM_017016275.1:c.423C>T	XP_016871764.1:p.Gly141=