Canonical Allele Identifier: CA1706662074
Gene: DDC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50561077G= , CM000669.2:g.50561077G= GRCh38
NC_000007.13:g.50628774G= , CM000669.1:g.50628774G= GRCh37
NC_000007.12:g.50596268G= NCBI36
NG_008742.1:g.9381C=

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.-29+4208C= MANE Select ENSP00000403644.2:n.-29+4208C=
ENST00000420203.1:c.-29+2918C= ENSP00000408626.1:n.-29+2918C=
ENST00000444124.6:c.-29+4208C= ENSP00000403644.2:n.-29+4208C=
NM_001082971.1:c.-29+4208C= NP_001076440.1:n.-29+4208C=
XM_005271745.3:c.-29+4208C= XP_005271802.1:n.-29+4208C=
XM_005271745.4:c.-29+4208C= XP_005271802.1:n.-29+4208C=
NM_001082971.2:c.-29+4208C= MANE Select NP_001076440.2:n.-29+4208C=
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