Canonical Allele Identifier: CA2611438369

Gene: MGMT

Linked Data

• gnomAD v4: 10-129767089-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767089G>A , CM000672.2:g.129767089G>A	GRCh38
NC_000010.10:g.131565353G>A , CM000672.1:g.131565353G>A	GRCh37
NC_000010.9:g.131455343G>A	NCBI36
NG_052673.1:g.304906G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*92G>A	ENSP00000302111.7:n.*92G>A
ENST00000651593.1:c.*92G>A MANE Select	ENSP00000498729.1:n.*92G>A
ENST00000306010.7:c.*92G>A	ENSP00000302111.7:n.*92G>A
NM_002412.3:c.*92G>A	NP_002403.2:n.*92G>A
NM_002412.4:c.*92G>A	NP_002403.2:n.*92G>A
XM_005252682.2:c.*92G>A	XP_005252739.1:n.*92G>A
XM_006717863.2:c.*92G>A	XP_006717926.1:n.*92G>A
XM_011539817.1:c.*92G>A	XP_011538119.1:n.*92G>A
NM_002412.5:c.*92G>A MANE Select	NP_002403.3:n.*92G>A
XM_017016275.1:c.*92G>A	XP_016871764.1:n.*92G>A