Canonical Allele Identifier: CA2611438368
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129767088-TG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767090del , CM000672.2:g.129767090del GRCh38
NC_000010.10:g.131565354del , CM000672.1:g.131565354del GRCh37
NC_000010.9:g.131455344del NCBI36
NG_052673.1:g.304907del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*93del ENSP00000302111.7:n.*93del
ENST00000651593.1:c.*93del MANE Select ENSP00000498729.1:n.*93del
ENST00000306010.7:c.*93del ENSP00000302111.7:n.*93del
NM_002412.3:c.*93del NP_002403.2:n.*93del
NM_002412.4:c.*93del NP_002403.2:n.*93del
XM_005252682.2:c.*93del XP_005252739.1:n.*93del
XM_006717863.2:c.*93del XP_006717926.1:n.*93del
XM_011539817.1:c.*93del XP_011538119.1:n.*93del
NM_002412.5:c.*93del MANE Select NP_002403.3:n.*93del
XM_017016275.1:c.*93del XP_016871764.1:n.*93del
Search 100 bp 5'
Search 100 bp 3'