Canonical Allele Identifier: CA1944760009
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129467293C= , CM000672.2:g.129467293C= GRCh38
NC_000010.10:g.131265557C= , CM000672.1:g.131265557C= GRCh37
NC_000010.9:g.131155547C= NCBI36
NG_052673.1:g.5110C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.78C= ENSP00000302111.7:p.Asp26=
ENST00000651593.1:c.-16C= MANE Select ENSP00000498729.1:n.-16C=
ENST00000306010.7:c.78C= ENSP00000302111.7:p.Asp26=
ENST00000482547.1:n.32C=
ENST00000482653.1:n.65C=
NM_002412.3:c.78C= NP_002403.2:p.Asp26=
NM_002412.4:c.78C= NP_002403.2:p.Asp26=
XM_005252682.2:c.-161C= XP_005252739.1:n.-161C=
NM_002412.5:c.-16C= MANE Select NP_002403.3:n.-16C=