Canonical Allele Identifier: CA715723
Gene: AHDC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2968472
ClinVar RCV Id: RCV003821598
dbSNP Id: rs776637247
gnomAD v2: 1-27875956-G-A
gnomAD v3: 1-27549445-G-A
gnomAD v4: 1-27549445-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27549445G>A , CM000663.2:g.27549445G>A GRCh38
NC_000001.10:g.27875956G>A , CM000663.1:g.27875956G>A GRCh37
NC_000001.9:g.27748543G>A NCBI36
NG_034158.1:g.59050C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247087.10:c.2671C>T ENSP00000247087.4:p.Arg891Trp
ENST00000642245.1:c.2671C>T ENSP00000495072.1:p.Arg891Trp
ENST00000642416.1:c.2671C>T ENSP00000494394.1:p.Arg891Trp
ENST00000644989.1:c.2671C>T ENSP00000495665.1:p.Arg891Trp
ENST00000673934.1:c.2671C>T MANE Select ENSP00000501218.1:p.Arg891Trp
ENST00000247087.9:c.2671C>T ENSP00000247087.4:p.Arg891Trp
ENST00000374011.6:c.2671C>T ENSP00000363123.2:p.Arg891Trp
NM_001029882.3:c.2671C>T NP_001025053.1:p.Arg891Trp
XM_005245848.2:c.2671C>T XP_005245905.1:p.Arg891Trp
XM_005245849.2:c.2671C>T XP_005245906.1:p.Arg891Trp
XM_005245850.2:c.2671C>T XP_005245907.1:p.Arg891Trp
XM_005245851.2:c.2671C>T XP_005245908.1:p.Arg891Trp
XM_005245852.2:c.2671C>T XP_005245909.1:p.Arg891Trp
XM_011541255.1:c.2671C>T XP_011539557.1:p.Arg891Trp
XM_011541256.1:c.2671C>T XP_011539558.1:p.Arg891Trp
XM_011541257.1:c.2671C>T XP_011539559.1:p.Arg891Trp
XR_946609.1:n.3628C>T
XM_005245848.3:c.2671C>T XP_005245905.1:p.Arg891Trp
XM_005245849.3:c.2671C>T XP_005245906.1:p.Arg891Trp
XM_005245850.3:c.2671C>T XP_005245907.1:p.Arg891Trp
XM_005245851.3:c.2671C>T XP_005245908.1:p.Arg891Trp
XM_005245852.3:c.2671C>T XP_005245909.1:p.Arg891Trp
XM_011541256.2:c.2671C>T XP_011539558.1:p.Arg891Trp
XM_011541257.2:c.2671C>T XP_011539559.1:p.Arg891Trp
XM_024446461.1:c.2671C>T XP_024302229.1:p.Arg891Trp
XR_946609.2:n.3738C>T
NM_001371928.1:c.2671C>T MANE Select NP_001358857.1:p.Arg891Trp