Canonical Allele Identifier: CA13175339

Gene: MGMT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129702676G>C , CM000672.2:g.129702676G>C	GRCh38
NC_000010.10:g.131500940G>C , CM000672.1:g.131500940G>C	GRCh37
NC_000010.9:g.131390930G>C	NCBI36
NG_052673.1:g.240493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.219-5219G>C	ENSP00000302111.7:n.219-5219G>C
ENST00000651593.1:c.126-5219G>C MANE Select	ENSP00000498729.1:n.126-5219G>C
ENST00000306010.7:c.219-5219G>C	ENSP00000302111.7:n.219-5219G>C
ENST00000462672.1:n.286+764G>C
NM_002412.3:c.219-5219G>C	NP_002403.2:n.219-5219G>C
NM_002412.4:c.219-5219G>C	NP_002403.2:n.219-5219G>C
XM_005252682.2:c.126-5219G>C	XP_005252739.1:n.126-5219G>C
XM_006717863.2:c.-52-5219G>C	XP_006717926.1:n.-52-5219G>C
XM_011539817.1:c.135-5219G>C	XP_011538119.1:n.135-5219G>C
NM_002412.5:c.126-5219G>C MANE Select	NP_002403.3:n.126-5219G>C
XM_017016275.1:c.-52-5219G>C	XP_016871764.1:n.-52-5219G>C