Canonical Allele Identifier: CA1706662076
Gene: DDC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50561079_50561082delinsACAG , CM000669.2:g.50561079_50561082delinsACAG GRCh38
NC_000007.13:g.50628776_50628779delinsACAG , CM000669.1:g.50628776_50628779delinsACAG GRCh37
NC_000007.12:g.50596270_50596273delinsACAG NCBI36
NG_008742.1:g.9376_9379delinsCTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.-29+4203_-29+4206delinsCTGT MANE Select ENSP00000403644.2:n.-29+4203_-29+4206delinsCTGT
ENST00000420203.1:c.-29+2913_-29+2916delinsCTGT ENSP00000408626.1:n.-29+2913_-29+2916delinsCTGT
ENST00000444124.6:c.-29+4203_-29+4206delinsCTGT ENSP00000403644.2:n.-29+4203_-29+4206delinsCTGT
NM_001082971.1:c.-29+4203_-29+4206delinsCTGT NP_001076440.1:n.-29+4203_-29+4206delinsCTGT
XM_005271745.3:c.-29+4203_-29+4206delinsCTGT XP_005271802.1:n.-29+4203_-29+4206delinsCTGT
XM_005271745.4:c.-29+4203_-29+4206delinsCTGT XP_005271802.1:n.-29+4203_-29+4206delinsCTGT
NM_001082971.2:c.-29+4203_-29+4206delinsCTGT MANE Select NP_001076440.2:n.-29+4203_-29+4206delinsCTGT