Canonical Allele Identifier: CA661571005
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1419614804
gnomAD v4: 10-129767115-TGC-T
MyVariant Identifiers: chr10:g.131565380_131565381del (hg19) chr10:g.129767116_129767117del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767116_129767117del , CM000672.2:g.129767116_129767117del GRCh38
NC_000010.10:g.131565380_131565381del , CM000672.1:g.131565380_131565381del GRCh37
NC_000010.9:g.131455370_131455371del NCBI36
NG_052673.1:g.304933_304934del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*119_*120del ENSP00000302111.7:n.*119_*120del
ENST00000651593.1:c.*119_*120del MANE Select ENSP00000498729.1:n.*119_*120del
ENST00000306010.7:c.*119_*120del ENSP00000302111.7:n.*119_*120del
NM_002412.3:c.*119_*120del NP_002403.2:n.*119_*120del
NM_002412.4:c.*119_*120del NP_002403.2:n.*119_*120del
XM_006717863.2:c.*119_*120del XP_006717926.1:n.*119_*120del
XM_011539817.1:c.*119_*120del XP_011538119.1:n.*119_*120del
NM_002412.5:c.*119_*120del MANE Select NP_002403.3:n.*119_*120del
XM_017016275.1:c.*119_*120del XP_016871764.1:n.*119_*120del
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