Canonical Allele Identifier: CA1944760527
Gene: MGMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129468212_129468213delinsAT , CM000672.2:g.129468212_129468213delinsAT GRCh38
NC_000010.10:g.131266476_131266477delinsAT , CM000672.1:g.131266476_131266477delinsAT GRCh37
NC_000010.9:g.131156466_131156467delinsAT NCBI36
NG_052673.1:g.6029_6030delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.81+916_81+917delinsAT ENSP00000302111.7:n.81+916_81+917delinsAT
ENST00000651593.1:c.-13+916_-13+917delinsAT MANE Select ENSP00000498729.1:n.-13+916_-13+917delinsAT
ENST00000306010.7:c.81+916_81+917delinsAT ENSP00000302111.7:n.81+916_81+917delinsAT
ENST00000482547.1:n.35+916_35+917delinsAT
ENST00000482653.1:n.68+916_68+917delinsAT
NM_002412.3:c.81+916_81+917delinsAT NP_002403.2:n.81+916_81+917delinsAT
NM_002412.4:c.81+916_81+917delinsAT NP_002403.2:n.81+916_81+917delinsAT
XM_005252682.2:c.-13+771_-13+772delinsAT XP_005252739.1:n.-13+771_-13+772delinsAT
NM_002412.5:c.-13+916_-13+917delinsAT MANE Select NP_002403.3:n.-13+916_-13+917delinsAT