Canonical Allele Identifier: CA1160545798
Gene: AHDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27550946_27550947delinsTG , CM000663.2:g.27550946_27550947delinsTG GRCh38
NC_000001.10:g.27877457_27877458delinsTG , CM000663.1:g.27877457_27877458delinsTG GRCh37
NC_000001.9:g.27750044_27750045delinsTG NCBI36
NG_034158.1:g.57548_57549delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000247087.10:c.1169_1170delinsCA ENSP00000247087.4:p.Pro390=
ENST00000642245.1:c.1169_1170delinsCA ENSP00000495072.1:p.Pro390=
ENST00000642416.1:c.1169_1170delinsCA ENSP00000494394.1:p.Pro390=
ENST00000643308.1:n.1983_1984delinsCA
ENST00000644989.1:c.1169_1170delinsCA ENSP00000495665.1:p.Pro390=
ENST00000673934.1:c.1169_1170delinsCA MANE Select ENSP00000501218.1:p.Pro390=
ENST00000247087.9:c.1169_1170delinsCA ENSP00000247087.4:p.Pro390=
ENST00000374011.6:c.1169_1170delinsCA ENSP00000363123.2:p.Pro390=
NM_001029882.3:c.1169_1170delinsCA NP_001025053.1:p.Pro390=
XM_005245848.2:c.1169_1170delinsCA XP_005245905.1:p.Pro390=
XM_005245849.2:c.1169_1170delinsCA XP_005245906.1:p.Pro390=
XM_005245850.2:c.1169_1170delinsCA XP_005245907.1:p.Pro390=
XM_005245851.2:c.1169_1170delinsCA XP_005245908.1:p.Pro390=
XM_005245852.2:c.1169_1170delinsCA XP_005245909.1:p.Pro390=
XM_011541255.1:c.1169_1170delinsCA XP_011539557.1:p.Pro390=
XM_011541256.1:c.1169_1170delinsCA XP_011539558.1:p.Pro390=
XM_011541257.1:c.1169_1170delinsCA XP_011539559.1:p.Pro390=
XR_946609.1:n.2126_2127delinsCA
XM_005245848.3:c.1169_1170delinsCA XP_005245905.1:p.Pro390=
XM_005245849.3:c.1169_1170delinsCA XP_005245906.1:p.Pro390=
XM_005245850.3:c.1169_1170delinsCA XP_005245907.1:p.Pro390=
XM_005245851.3:c.1169_1170delinsCA XP_005245908.1:p.Pro390=
XM_005245852.3:c.1169_1170delinsCA XP_005245909.1:p.Pro390=
XM_011541256.2:c.1169_1170delinsCA XP_011539558.1:p.Pro390=
XM_011541257.2:c.1169_1170delinsCA XP_011539559.1:p.Pro390=
XM_024446461.1:c.1169_1170delinsCA XP_024302229.1:p.Pro390=
XR_946609.2:n.2236_2237delinsCA
NM_001371928.1:c.1169_1170delinsCA MANE Select NP_001358857.1:p.Pro390=