Canonical Allele Identifier: CA367538181

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50495417A>T , CM000669.2:g.50495417A>T GRCh38
NC_000007.13:g.50563115A>T , CM000669.1:g.50563115A>T GRCh37
NC_000007.12:g.50530609A>T NCBI36
NG_008742.1:g.75040T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000444124.7:c.877T>A (DDC) MANE Select ENSP00000403644.2:p.Phe293Ile
ENST00000357936.9:c.877T>A (DDC) ENSP00000350616.5:p.Phe293Ile
ENST00000380984.4:c.877T>A (DDC) ENSP00000370371.4:p.Phe293Ile
ENST00000426377.5:c.643T>A (DDC) ENSP00000395069.1:p.Phe215Ile
ENST00000430300.5:c.519T>A (DDC)
ENST00000431062.5:c.598T>A (DDC) ENSP00000399184.1:p.Phe200Ile
ENST00000444124.6:c.877T>A (DDC) ENSP00000403644.2:p.Phe293Ile
ENST00000444733.5:c.668T>A (DDC) ENSP00000393724.1:p.Phe223Tyr
ENST00000613602.3:c.-11+47101T>A (FIGNL1) ENSP00000481751.1:n.-11+47101T>A
ENST00000615193.4:c.598T>A (DDC) ENSP00000484104.1:p.Phe200Ile
ENST00000617822.4:c.733T>A (DDC) ENSP00000478385.1:p.Phe245Ile
ENST00000622873.4:c.763T>A (DDC) ENSP00000479110.1:p.Phe255Ile
NM_000790.3:c.877T>A (DDC) NP_000781.1:p.Phe293Ile
NM_001082971.1:c.877T>A (DDC) NP_001076440.1:p.Phe293Ile
NM_001242886.1:c.763T>A (DDC) NP_001229815.1:p.Phe255Ile
NM_001242887.1:c.733T>A (DDC) NP_001229816.1:p.Phe245Ile
NM_001242888.1:c.643T>A (DDC) NP_001229817.1:p.Phe215Ile
NM_001242889.1:c.598T>A (DDC) NP_001229818.1:p.Phe200Ile
NM_001242890.1:c.877T>A (DDC) NP_001229819.1:p.Phe293Ile
XM_005271745.3:c.763T>A (DDC) XP_005271802.1:p.Phe255Ile
XM_011515161.1:c.526T>A (DDC) XP_011513463.1:p.Phe176Ile
XM_005271745.4:c.763T>A (DDC) XP_005271802.1:p.Phe255Ile
XM_011515161.2:c.820T>A (DDC) XP_011513463.2:p.Phe274Ile
NM_001082971.2:c.877T>A (DDC) MANE Select NP_001076440.2:p.Phe293Ile
NM_000790.4:c.877T>A (DDC) NP_000781.2:p.Phe293Ile
NM_001242888.2:c.643T>A (DDC) NP_001229817.2:p.Phe215Ile
NM_001242890.2:c.877T>A (DDC) NP_001229819.2:p.Phe293Ile
NM_001242886.2:c.763T>A (DDC) NP_001229815.2:p.Phe255Ile
NM_001242887.2:c.733T>A (DDC) NP_001229816.2:p.Phe245Ile
NM_001242889.2:c.598T>A (DDC) NP_001229818.2:p.Phe200Ile