Canonical Allele Identifier: CA1944891386

Gene: MGMT

Linked Data

• dbSNP Id: rs1848946091

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129766989del , CM000672.2:g.129766989del	GRCh38
NC_000010.10:g.131565253del , CM000672.1:g.131565253del	GRCh37
NC_000010.9:g.131455243del	NCBI36
NG_052673.1:g.304806del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.709del	ENSP00000302111.7:p.Arg237GlufsTer7
ENST00000651593.1:c.616del MANE Select	ENSP00000498729.1:p.Arg206GlufsTer7
ENST00000306010.7:c.709del	ENSP00000302111.7:p.Arg237GlufsTer7
NM_002412.3:c.709del	NP_002403.2:p.Arg237GlufsTer7
NM_002412.4:c.709del	NP_002403.2:p.Arg237GlufsTer7
XM_005252682.2:c.616del	XP_005252739.1:p.Arg206GlufsTer7
XM_006717863.2:c.439del	XP_006717926.1:p.Arg147GlufsTer7
XM_011539817.1:c.625del	XP_011538119.1:p.Arg209GlufsTer7
NM_002412.5:c.616del MANE Select	NP_002403.3:p.Arg206GlufsTer7
XM_017016275.1:c.439del	XP_016871764.1:p.Arg147GlufsTer7