Canonical Allele Identifier: CA1944862155
Community Standard Title: NM_002412.5(MGMT):c.126-5219G=
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129702676G= , CM000672.2:g.129702676G= GRCh38
NC_000010.10:g.131500940G= , CM000672.1:g.131500940G= GRCh37
NC_000010.9:g.131390930G= NCBI36
NG_052673.1:g.240493G=

Transcript Alleles

HGVS Amino-acid Change
NM_002412.5:c.126-5219G= MANE Select NP_002403.3:n.126-5219G=
ENST00000651593.1:c.126-5219G= MANE Select ENSP00000498729.1:n.126-5219G=
NM_002412.3:c.219-5219G= NP_002403.2:n.219-5219G=
NM_002412.4:c.219-5219G= NP_002403.2:n.219-5219G=
ENST00000306010.7:c.219-5219G= ENSP00000302111.7:n.219-5219G=
ENST00000306010.8:c.219-5219G= ENSP00000302111.7:n.219-5219G=
ENST00000462672.1:n.286+764G=
XM_005252682.2:c.126-5219G= XP_005252739.1:n.126-5219G=
XM_006717863.2:c.-52-5219G= XP_006717926.1:n.-52-5219G=
XM_011539817.1:c.135-5219G= XP_011538119.1:n.135-5219G=
XM_017016275.1:c.-52-5219G= XP_016871764.1:n.-52-5219G=