Canonical Allele Identifier: CA216018196

Gene: MGMT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129691518A>C , CM000672.2:g.129691518A>C	GRCh38
NC_000010.10:g.131489782A>C , CM000672.1:g.131489782A>C	GRCh37
NC_000010.9:g.131379772A>C	NCBI36
NG_052673.1:g.229335A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.219-16377A>C	ENSP00000302111.7:n.219-16377A>C
ENST00000651593.1:c.126-16377A>C MANE Select	ENSP00000498729.1:n.126-16377A>C
ENST00000306010.7:c.219-16377A>C	ENSP00000302111.7:n.219-16377A>C
NM_002412.3:c.219-16377A>C	NP_002403.2:n.219-16377A>C
NM_002412.4:c.219-16377A>C	NP_002403.2:n.219-16377A>C
XM_005252682.2:c.126-16377A>C	XP_005252739.1:n.126-16377A>C
XM_006717863.2:c.-52-16377A>C	XP_006717926.1:n.-52-16377A>C
XM_011539817.1:c.135-16377A>C	XP_011538119.1:n.135-16377A>C
NM_002412.5:c.126-16377A>C MANE Select	NP_002403.3:n.126-16377A>C
XM_017016275.1:c.-52-16377A>C	XP_016871764.1:n.-52-16377A>C