Canonical Allele Identifier: CA319658
Gene: AHDC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208156
ClinVar RCV Id: RCV000190361
dbSNP Id: rs796065040

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27550235del , CM000663.2:g.27550235del GRCh38
NC_000001.10:g.27876746del , CM000663.1:g.27876746del GRCh37
NC_000001.9:g.27749333del NCBI36
NG_034158.1:g.58260del

Transcript Alleles

HGVS Amino-acid change
ENST00000247087.10:c.1881del ENSP00000247087.4:p.Gln627HisfsTer?
ENST00000642245.1:c.1881del ENSP00000495072.1:p.Gln627HisfsTer?
ENST00000642416.1:c.1881del ENSP00000494394.1:p.Gln627HisfsTer?
ENST00000644989.1:c.1881del ENSP00000495665.1:p.Gln627HisfsTer?
ENST00000673934.1:c.1881del MANE Select ENSP00000501218.1:p.Gln627HisfsTer?
ENST00000247087.9:c.1881del ENSP00000247087.4:p.Gln627HisfsTer?
ENST00000374011.6:c.1881del ENSP00000363123.2:p.Gln627HisfsTer?
NM_001029882.3:c.1881del NP_001025053.1:p.Gln627HisfsTer?
XM_005245848.2:c.1881del XP_005245905.1:p.Gln627HisfsTer?
XM_005245849.2:c.1881del XP_005245906.1:p.Gln627HisfsTer?
XM_005245850.2:c.1881del XP_005245907.1:p.Gln627HisfsTer?
XM_005245851.2:c.1881del XP_005245908.1:p.Gln627HisfsTer?
XM_005245852.2:c.1881del XP_005245909.1:p.Gln627HisfsTer?
XM_011541255.1:c.1881del XP_011539557.1:p.Gln627HisfsTer?
XM_011541256.1:c.1881del XP_011539558.1:p.Gln627HisfsTer?
XM_011541257.1:c.1881del XP_011539559.1:p.Gln627HisfsTer?
XR_946609.1:n.2838del
XM_005245848.3:c.1881del XP_005245905.1:p.Gln627HisfsTer?
XM_005245849.3:c.1881del XP_005245906.1:p.Gln627HisfsTer?
XM_005245850.3:c.1881del XP_005245907.1:p.Gln627HisfsTer?
XM_005245851.3:c.1881del XP_005245908.1:p.Gln627HisfsTer?
XM_005245852.3:c.1881del XP_005245909.1:p.Gln627HisfsTer?
XM_011541256.2:c.1881del XP_011539558.1:p.Gln627HisfsTer?
XM_011541257.2:c.1881del XP_011539559.1:p.Gln627HisfsTer?
XM_024446461.1:c.1881del XP_024302229.1:p.Gln627HisfsTer?
XR_946609.2:n.2948del
NM_001371928.1:c.1881del MANE Select NP_001358857.1:p.Gln627HisfsTer?