Canonical Allele Identifier: CA10602798
Gene: AHDC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280482
dbSNP Id: rs886041676

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27549425del , CM000663.2:g.27549425del GRCh38
NC_000001.10:g.27875936del , CM000663.1:g.27875936del GRCh37
NC_000001.9:g.27748523del NCBI36
NG_034158.1:g.59070del

Transcript Alleles

HGVS Amino-acid Change
ENST00000247087.10:c.2691del ENSP00000247087.4:p.Val898TrpfsTer?
ENST00000642245.1:c.2691del ENSP00000495072.1:p.Val898TrpfsTer?
ENST00000642416.1:c.2691del ENSP00000494394.1:p.Val898TrpfsTer?
ENST00000644989.1:c.2691del ENSP00000495665.1:p.Val898TrpfsTer?
ENST00000673934.1:c.2691del MANE Select ENSP00000501218.1:p.Val898TrpfsTer?
ENST00000247087.9:c.2691del ENSP00000247087.4:p.Val898TrpfsTer?
ENST00000374011.6:c.2691del ENSP00000363123.2:p.Val898TrpfsTer?
NM_001029882.3:c.2691del NP_001025053.1:p.Val898TrpfsTer?
XM_005245848.2:c.2691del XP_005245905.1:p.Val898TrpfsTer?
XM_005245849.2:c.2691del XP_005245906.1:p.Val898TrpfsTer?
XM_005245850.2:c.2691del XP_005245907.1:p.Val898TrpfsTer?
XM_005245851.2:c.2691del XP_005245908.1:p.Val898TrpfsTer?
XM_005245852.2:c.2691del XP_005245909.1:p.Val898TrpfsTer?
XM_011541255.1:c.2691del XP_011539557.1:p.Val898TrpfsTer?
XM_011541256.1:c.2691del XP_011539558.1:p.Val898TrpfsTer?
XM_011541257.1:c.2691del XP_011539559.1:p.Val898TrpfsTer?
XR_946609.1:n.3648del
XM_005245848.3:c.2691del XP_005245905.1:p.Val898TrpfsTer?
XM_005245849.3:c.2691del XP_005245906.1:p.Val898TrpfsTer?
XM_005245850.3:c.2691del XP_005245907.1:p.Val898TrpfsTer?
XM_005245851.3:c.2691del XP_005245908.1:p.Val898TrpfsTer?
XM_005245852.3:c.2691del XP_005245909.1:p.Val898TrpfsTer?
XM_011541256.2:c.2691del XP_011539558.1:p.Val898TrpfsTer?
XM_011541257.2:c.2691del XP_011539559.1:p.Val898TrpfsTer?
XM_024446461.1:c.2691del XP_024302229.1:p.Val898TrpfsTer?
XR_946609.2:n.3758del
NM_001371928.1:c.2691del MANE Select NP_001358857.1:p.Val898TrpfsTer?