Canonical Allele Identifier: CA2574707796
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129766816_129766817dup , CM000672.2:g.129766816_129766817dup GRCh38
NC_000010.10:g.131565080_131565081dup , CM000672.1:g.131565080_131565081dup GRCh37
NC_000010.9:g.131455070_131455071dup NCBI36
NG_052673.1:g.304633_304634dup

Transcript Alleles

HGVS Amino-acid change
ENST00000306010.8:c.536_537dup ENSP00000302111.7:p.Val180TrpfsTer17
ENST00000651593.1:c.443_444dup MANE Select ENSP00000498729.1:p.Val149TrpfsTer17
ENST00000306010.7:c.536_537dup ENSP00000302111.7:p.Val180TrpfsTer17
NM_002412.3:c.536_537dup NP_002403.2:p.Val180TrpfsTer17
NM_002412.4:c.536_537dup NP_002403.2:p.Val180TrpfsTer17
XM_005252682.2:c.443_444dup XP_005252739.1:p.Val149TrpfsTer17
XM_006717863.2:c.266_267dup XP_006717926.1:p.Val90TrpfsTer17
XM_011539817.1:c.452_453dup XP_011538119.1:p.Val152TrpfsTer17
NM_002412.5:c.443_444dup MANE Select NP_002403.3:p.Val149TrpfsTer17
XM_017016275.1:c.266_267dup XP_016871764.1:p.Val90TrpfsTer17