Canonical Allele Identifier: CA661570996
Gene: MGMT HGNC NCBI

Linked Data

dbSNP Id: rs1273118406
gnomAD v3: 10-129767099-TG-T
gnomAD v4: 10-129767099-TG-T
MyVariant Identifiers: chr10:g.131565364del (hg19) chr10:g.129767100del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129767102del , CM000672.2:g.129767102del GRCh38
NC_000010.10:g.131565366del , CM000672.1:g.131565366del GRCh37
NC_000010.9:g.131455356del NCBI36
NG_052673.1:g.304919del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306010.8:c.*105del ENSP00000302111.7:n.*105del
ENST00000651593.1:c.*105del MANE Select ENSP00000498729.1:n.*105del
ENST00000306010.7:c.*105del ENSP00000302111.7:n.*105del
NM_002412.3:c.*105del NP_002403.2:n.*105del
NM_002412.4:c.*105del NP_002403.2:n.*105del
XM_005252682.2:c.*105del XP_005252739.1:n.*105del
XM_006717863.2:c.*105del XP_006717926.1:n.*105del
XM_011539817.1:c.*105del XP_011538119.1:n.*105del
NM_002412.5:c.*105del MANE Select NP_002403.3:n.*105del
XM_017016275.1:c.*105del XP_016871764.1:n.*105del
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