Canonical Allele Identifier: CA1944891233
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766930G= , CM000672.2:g.129766930G= GRCh38
NC_000010.10:g.131565194G= , CM000672.1:g.131565194G= GRCh37
NC_000010.9:g.131455184G= NCBI36
NG_052673.1:g.304747G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.650G= ENSP00000302111.7:p.Gly217=
ENST00000651593.1:c.557G= MANE Select ENSP00000498729.1:p.Gly186=
ENST00000306010.7:c.650G= ENSP00000302111.7:p.Gly217=
NM_002412.3:c.650G= NP_002403.2:p.Gly217=
NM_002412.4:c.650G= NP_002403.2:p.Gly217=
XM_005252682.2:c.557G= XP_005252739.1:p.Gly186=
XM_006717863.2:c.380G= XP_006717926.1:p.Gly127=
XM_011539817.1:c.566G= XP_011538119.1:p.Gly189=
NM_002412.5:c.557G= MANE Select NP_002403.3:p.Gly186=
XM_017016275.1:c.380G= XP_016871764.1:p.Gly127=