Canonical Allele Identifier: CA2611438246

Gene: MGMT

Linked Data

• gnomAD v4: 10-129766712-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766712C>A , CM000672.2:g.129766712C>A	GRCh38
NC_000010.10:g.131564976C>A , CM000672.1:g.131564976C>A	GRCh37
NC_000010.9:g.131454966C>A	NCBI36
NG_052673.1:g.304529C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.508-76C>A	ENSP00000302111.7:n.508-76C>A
ENST00000651593.1:c.415-76C>A MANE Select	ENSP00000498729.1:n.415-76C>A
ENST00000306010.7:c.508-76C>A	ENSP00000302111.7:n.508-76C>A
NM_002412.3:c.508-76C>A	NP_002403.2:n.508-76C>A
NM_002412.4:c.508-76C>A	NP_002403.2:n.508-76C>A
XM_005252682.2:c.415-76C>A	XP_005252739.1:n.415-76C>A
XM_006717863.2:c.238-76C>A	XP_006717926.1:n.238-76C>A
XM_011539817.1:c.424-76C>A	XP_011538119.1:n.424-76C>A
NM_002412.5:c.415-76C>A MANE Select	NP_002403.3:n.415-76C>A
XM_017016275.1:c.238-76C>A	XP_016871764.1:n.238-76C>A