Canonical Allele Identifier: CA1944760526

Gene: MGMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129468212_129468214delinsATG , CM000672.2:g.129468212_129468214delinsATG	GRCh38
NC_000010.10:g.131266476_131266478delinsATG , CM000672.1:g.131266476_131266478delinsATG	GRCh37
NC_000010.9:g.131156466_131156468delinsATG	NCBI36
NG_052673.1:g.6029_6031delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.81+916_81+918delinsATG	ENSP00000302111.7:n.81+916_81+918delinsATG
ENST00000651593.1:c.-13+916_-13+918delinsATG MANE Select	ENSP00000498729.1:n.-13+916_-13+918delinsATG
ENST00000306010.7:c.81+916_81+918delinsATG	ENSP00000302111.7:n.81+916_81+918delinsATG
ENST00000482547.1:n.35+916_35+918delinsATG
ENST00000482653.1:n.68+916_68+918delinsATG
NM_002412.3:c.81+916_81+918delinsATG	NP_002403.2:n.81+916_81+918delinsATG
NM_002412.4:c.81+916_81+918delinsATG	NP_002403.2:n.81+916_81+918delinsATG
XM_005252682.2:c.-13+771_-13+773delinsATG	XP_005252739.1:n.-13+771_-13+773delinsATG
NM_002412.5:c.-13+916_-13+918delinsATG MANE Select	NP_002403.3:n.-13+916_-13+918delinsATG