Canonical Allele Identifier: CA471816677

Gene: MGMT

Linked Data

• MyVariant Identifiers: chr10:g.131565243G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766979G>C , CM000672.2:g.129766979G>C	GRCh38
NC_000010.10:g.131565243G>C , CM000672.1:g.131565243G>C	GRCh37
NC_000010.9:g.131455233G>C	NCBI36
NG_052673.1:g.304796G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.699G>C	ENSP00000302111.7:p.Pro233=
ENST00000651593.1:c.606G>C MANE Select	ENSP00000498729.1:p.Pro202=
ENST00000306010.7:c.699G>C	ENSP00000302111.7:p.Pro233=
NM_002412.3:c.699G>C	NP_002403.2:p.Pro233=
NM_002412.4:c.699G>C	NP_002403.2:p.Pro233=
XM_005252682.2:c.606G>C	XP_005252739.1:p.Pro202=
XM_006717863.2:c.429G>C	XP_006717926.1:p.Pro143=
XM_011539817.1:c.615G>C	XP_011538119.1:p.Pro205=
NM_002412.5:c.606G>C MANE Select	NP_002403.3:p.Pro202=
XM_017016275.1:c.429G>C	XP_016871764.1:p.Pro143=