Canonical Allele Identifier: CA367526616

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50529216A>C , CM000669.2:g.50529216A>C GRCh38
NC_000007.13:g.50596914A>C , CM000669.1:g.50596914A>C GRCh37
NC_000007.12:g.50564408A>C NCBI36
NG_008742.1:g.41241T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000444124.7:c.562T>G (DDC) MANE Select ENSP00000403644.2:p.Ser188Ala
ENST00000357936.9:c.562T>G (DDC) ENSP00000350616.5:p.Ser188Ala
ENST00000380984.4:c.562T>G (DDC) ENSP00000370371.4:p.Ser188Ala
ENST00000426377.5:c.328T>G (DDC) ENSP00000395069.1:p.Ser110Ala
ENST00000430300.5:c.213-936T>G (DDC)
ENST00000431062.5:c.435+8644T>G (DDC) ENSP00000399184.1:n.435+8644T>G
ENST00000444124.6:c.562T>G (DDC) ENSP00000403644.2:p.Ser188Ala
ENST00000444733.5:c.448T>G (DDC) ENSP00000393724.1:p.Ser150Ala
ENST00000489162.1:n.361T>G (DDC)
ENST00000613602.3:c.-11+13302T>G (FIGNL1) ENSP00000481751.1:n.-11+13302T>G
ENST00000615193.4:c.435+8644T>G (DDC) ENSP00000484104.1:n.435+8644T>G
ENST00000617822.4:c.562T>G (DDC) ENSP00000478385.1:p.Ser188Ala
ENST00000622873.4:c.448T>G (DDC) ENSP00000479110.1:p.Ser150Ala
NM_000790.3:c.562T>G (DDC) NP_000781.1:p.Ser188Ala
NM_001082971.1:c.562T>G (DDC) NP_001076440.1:p.Ser188Ala
NM_001242886.1:c.448T>G (DDC) NP_001229815.1:p.Ser150Ala
NM_001242887.1:c.562T>G (DDC) NP_001229816.1:p.Ser188Ala
NM_001242888.1:c.328T>G (DDC) NP_001229817.1:p.Ser110Ala
NM_001242889.1:c.435+8644T>G (DDC) NP_001229818.1:n.435+8644T>G
NM_001242890.1:c.562T>G (DDC) NP_001229819.1:p.Ser188Ala
XM_005271745.3:c.448T>G (DDC) XP_005271802.1:p.Ser150Ala
XM_011515161.1:c.211T>G (DDC) XP_011513463.1:p.Ser71Ala
XM_005271745.4:c.448T>G (DDC) XP_005271802.1:p.Ser150Ala
XM_011515161.2:c.505T>G (DDC) XP_011513463.2:p.Ser169Ala
NM_001082971.2:c.562T>G (DDC) MANE Select NP_001076440.2:p.Ser188Ala
NM_000790.4:c.562T>G (DDC) NP_000781.2:p.Ser188Ala
NM_001242888.2:c.328T>G (DDC) NP_001229817.2:p.Ser110Ala
NM_001242890.2:c.562T>G (DDC) NP_001229819.2:p.Ser188Ala
NM_001242886.2:c.448T>G (DDC) NP_001229815.2:p.Ser150Ala
NM_001242887.2:c.562T>G (DDC) NP_001229816.2:p.Ser188Ala
NM_001242889.2:c.435+8644T>G (DDC) NP_001229818.2:n.435+8644T>G