Canonical Allele Identifier: CA918789890

Gene: MGMT

Linked Data

• dbSNP Id: rs1589984291

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.129767121_129767124del , CM000672.2:g.129767121_129767124del	GRCh38
NC_000010.10:g.131565385_131565388del , CM000672.1:g.131565385_131565388del	GRCh37
NC_000010.9:g.131455375_131455378del	NCBI36
NG_052673.1:g.304938_304941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306010.8:c.*124_*127del	ENSP00000302111.7:n.*124_*127del
ENST00000651593.1:c.*124_*127del MANE Select	ENSP00000498729.1:n.*124_*127del
ENST00000306010.7:c.*124_*127del	ENSP00000302111.7:n.*124_*127del
NM_002412.3:c.*124_*127del	NP_002403.2:n.*124_*127del
NM_002412.4:c.*124_*127del	NP_002403.2:n.*124_*127del
XM_006717863.2:c.*124_*127del	XP_006717926.1:n.*124_*127del
XM_011539817.1:c.*124_*127del	XP_011538119.1:n.*124_*127del
NM_002412.5:c.*124_*127del MANE Select	NP_002403.3:n.*124_*127del
XM_017016275.1:c.*124_*127del	XP_016871764.1:n.*124_*127del