Canonical Allele Identifier: CA367526637

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50529225C>A , CM000669.2:g.50529225C>A GRCh38
NC_000007.13:g.50596923C>A , CM000669.1:g.50596923C>A GRCh37
NC_000007.12:g.50564417C>A NCBI36
NG_008742.1:g.41232G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000444124.7:c.553G>T (DDC) MANE Select ENSP00000403644.2:p.Ala185Ser
ENST00000357936.9:c.553G>T (DDC) ENSP00000350616.5:p.Ala185Ser
ENST00000380984.4:c.553G>T (DDC) ENSP00000370371.4:p.Ala185Ser
ENST00000426377.5:c.319G>T (DDC) ENSP00000395069.1:p.Ala107Ser
ENST00000430300.5:c.213-945G>T (DDC)
ENST00000431062.5:c.435+8635G>T (DDC) ENSP00000399184.1:n.435+8635G>T
ENST00000444124.6:c.553G>T (DDC) ENSP00000403644.2:p.Ala185Ser
ENST00000444733.5:c.439G>T (DDC) ENSP00000393724.1:p.Ala147Ser
ENST00000489162.1:n.352G>T (DDC)
ENST00000613602.3:c.-11+13293G>T (FIGNL1) ENSP00000481751.1:n.-11+13293G>T
ENST00000615193.4:c.435+8635G>T (DDC) ENSP00000484104.1:n.435+8635G>T
ENST00000617822.4:c.553G>T (DDC) ENSP00000478385.1:p.Ala185Ser
ENST00000622873.4:c.439G>T (DDC) ENSP00000479110.1:p.Ala147Ser
NM_000790.3:c.553G>T (DDC) NP_000781.1:p.Ala185Ser
NM_001082971.1:c.553G>T (DDC) NP_001076440.1:p.Ala185Ser
NM_001242886.1:c.439G>T (DDC) NP_001229815.1:p.Ala147Ser
NM_001242887.1:c.553G>T (DDC) NP_001229816.1:p.Ala185Ser
NM_001242888.1:c.319G>T (DDC) NP_001229817.1:p.Ala107Ser
NM_001242889.1:c.435+8635G>T (DDC) NP_001229818.1:n.435+8635G>T
NM_001242890.1:c.553G>T (DDC) NP_001229819.1:p.Ala185Ser
XM_005271745.3:c.439G>T (DDC) XP_005271802.1:p.Ala147Ser
XM_011515161.1:c.202G>T (DDC) XP_011513463.1:p.Ala68Ser
XM_005271745.4:c.439G>T (DDC) XP_005271802.1:p.Ala147Ser
XM_011515161.2:c.496G>T (DDC) XP_011513463.2:p.Ala166Ser
NM_001082971.2:c.553G>T (DDC) MANE Select NP_001076440.2:p.Ala185Ser
NM_000790.4:c.553G>T (DDC) NP_000781.2:p.Ala185Ser
NM_001242888.2:c.319G>T (DDC) NP_001229817.2:p.Ala107Ser
NM_001242890.2:c.553G>T (DDC) NP_001229819.2:p.Ala185Ser
NM_001242886.2:c.439G>T (DDC) NP_001229815.2:p.Ala147Ser
NM_001242887.2:c.553G>T (DDC) NP_001229816.2:p.Ala185Ser
NM_001242889.2:c.435+8635G>T (DDC) NP_001229818.2:n.435+8635G>T