Canonical Allele Identifier: CA1944921593
Community Standard Title: NM_002412.5(MGMT):c.427A= (p.Ile143=)
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766800A= , CM000672.2:g.129766800A= GRCh38
NC_000010.10:g.131565064A= , CM000672.1:g.131565064A= GRCh37
NC_000010.9:g.131455054A= NCBI36
NG_052673.1:g.304617A=

Transcript Alleles

HGVS Amino-acid Change
NM_002412.5:c.427A= MANE Select NP_002403.3:p.Ile143=
ENST00000651593.1:c.427A= MANE Select ENSP00000498729.1:p.Ile143=
NM_002412.3:c.520A= NP_002403.2:p.Ile174=
NM_002412.4:c.520A= NP_002403.2:p.Ile174=
ENST00000306010.7:c.520A= ENSP00000302111.7:p.Ile174=
ENST00000306010.8:c.520A= ENSP00000302111.7:p.Ile174=
XM_005252682.2:c.427A= XP_005252739.1:p.Ile143=
XM_006717863.2:c.250A= XP_006717926.1:p.Ile84=
XM_011539817.1:c.436A= XP_011538119.1:p.Ile146=
XM_017016275.1:c.250A= XP_016871764.1:p.Ile84=