Canonical Allele Identifier: CA653901311

Gene: MGMT

Linked Data

• COSMIC: COSN18734820 ; COSN18734821

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767027dup , CM000672.2:g.129767027dup	GRCh38
NC_000010.10:g.131565291dup , CM000672.1:g.131565291dup	GRCh37
NC_000010.9:g.131455281dup	NCBI36
NG_052673.1:g.304844dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*30dup	ENSP00000302111.7:n.*30dup
ENST00000651593.1:c.*30dup MANE Select	ENSP00000498729.1:n.*30dup
ENST00000306010.7:c.*30dup	ENSP00000302111.7:n.*30dup
NM_002412.3:c.*30dup	NP_002403.2:n.*30dup
NM_002412.4:c.*30dup	NP_002403.2:n.*30dup
XM_005252682.2:c.*30dup	XP_005252739.1:n.*30dup
XM_006717863.2:c.*30dup	XP_006717926.1:n.*30dup
XM_011539817.1:c.*30dup	XP_011538119.1:n.*30dup
NM_002412.5:c.*30dup MANE Select	NP_002403.3:n.*30dup
XM_017016275.1:c.*30dup	XP_016871764.1:n.*30dup