Canonical Allele Identifier: CA339232769
Gene: AHDC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438276
dbSNP Id: rs1165205177
gnomAD v4: 1-27550054-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27550054G>A , CM000663.2:g.27550054G>A GRCh38
NC_000001.10:g.27876565G>A , CM000663.1:g.27876565G>A GRCh37
NC_000001.9:g.27749152G>A NCBI36
NG_034158.1:g.58441C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000247087.10:c.2062C>T ENSP00000247087.4:p.Arg688Ter
ENST00000642245.1:c.2062C>T ENSP00000495072.1:p.Arg688Ter
ENST00000642416.1:c.2062C>T ENSP00000494394.1:p.Arg688Ter
ENST00000644989.1:c.2062C>T ENSP00000495665.1:p.Arg688Ter
ENST00000673934.1:c.2062C>T MANE Select ENSP00000501218.1:p.Arg688Ter
ENST00000247087.9:c.2062C>T ENSP00000247087.4:p.Arg688Ter
ENST00000374011.6:c.2062C>T ENSP00000363123.2:p.Arg688Ter
NM_001029882.3:c.2062C>T NP_001025053.1:p.Arg688Ter
XM_005245848.2:c.2062C>T XP_005245905.1:p.Arg688Ter
XM_005245849.2:c.2062C>T XP_005245906.1:p.Arg688Ter
XM_005245850.2:c.2062C>T XP_005245907.1:p.Arg688Ter
XM_005245851.2:c.2062C>T XP_005245908.1:p.Arg688Ter
XM_005245852.2:c.2062C>T XP_005245909.1:p.Arg688Ter
XM_011541255.1:c.2062C>T XP_011539557.1:p.Arg688Ter
XM_011541256.1:c.2062C>T XP_011539558.1:p.Arg688Ter
XM_011541257.1:c.2062C>T XP_011539559.1:p.Arg688Ter
XR_946609.1:n.3019C>T
XM_005245848.3:c.2062C>T XP_005245905.1:p.Arg688Ter
XM_005245849.3:c.2062C>T XP_005245906.1:p.Arg688Ter
XM_005245850.3:c.2062C>T XP_005245907.1:p.Arg688Ter
XM_005245851.3:c.2062C>T XP_005245908.1:p.Arg688Ter
XM_005245852.3:c.2062C>T XP_005245909.1:p.Arg688Ter
XM_011541256.2:c.2062C>T XP_011539558.1:p.Arg688Ter
XM_011541257.2:c.2062C>T XP_011539559.1:p.Arg688Ter
XM_024446461.1:c.2062C>T XP_024302229.1:p.Arg688Ter
XR_946609.2:n.3129C>T
NM_001371928.1:c.2062C>T MANE Select NP_001358857.1:p.Arg688Ter