Canonical Allele Identifier: CA2611438432
Gene: MGMT HGNC NCBI

Linked Data

gnomAD v4: 10-129767168-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767169del , CM000672.2:g.129767169del GRCh38
NC_000010.10:g.131565433del , CM000672.1:g.131565433del GRCh37
NC_000010.9:g.131455423del NCBI36
NG_052673.1:g.304986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*172del ENSP00000302111.7:n.*172del
ENST00000651593.1:c.*172del MANE Select ENSP00000498729.1:n.*172del
ENST00000306010.7:c.*172del ENSP00000302111.7:n.*172del
NM_002412.3:c.*172del NP_002403.2:n.*172del
NM_002412.4:c.*172del NP_002403.2:n.*172del
XM_006717863.2:c.*172del XP_006717926.1:n.*172del
XM_011539817.1:c.*172del XP_011538119.1:n.*172del
NM_002412.5:c.*172del MANE Select NP_002403.3:n.*172del
XM_017016275.1:c.*172del XP_016871764.1:n.*172del
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