Canonical Allele Identifier: CA653901320

Gene: MGMT

Linked Data

• COSMIC: COSN22493058

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767056_129767057insC , CM000672.2:g.129767056_129767057insC	GRCh38
NC_000010.10:g.131565320_131565321insC , CM000672.1:g.131565320_131565321insC	GRCh37
NC_000010.9:g.131455310_131455311insC	NCBI36
NG_052673.1:g.304873_304874insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*59_*60insC	ENSP00000302111.7:n.*59_*60insC
ENST00000651593.1:c.*59_*60insC MANE Select	ENSP00000498729.1:n.*59_*60insC
ENST00000306010.7:c.*59_*60insC	ENSP00000302111.7:n.*59_*60insC
NM_002412.3:c.*59_*60insC	NP_002403.2:n.*59_*60insC
NM_002412.4:c.*59_*60insC	NP_002403.2:n.*59_*60insC
XM_005252682.2:c.*59_*60insC	XP_005252739.1:n.*59_*60insC
XM_006717863.2:c.*59_*60insC	XP_006717926.1:n.*59_*60insC
XM_011539817.1:c.*59_*60insC	XP_011538119.1:n.*59_*60insC
NM_002412.5:c.*59_*60insC MANE Select	NP_002403.3:n.*59_*60insC
XM_017016275.1:c.*59_*60insC	XP_016871764.1:n.*59_*60insC