Canonical Allele Identifier: CA4262298
Community Standard Title: NM_001082971.2(DDC):c.710T>C (p.Phe237Ser)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50528141A>G , CM000669.2:g.50528141A>G GRCh38
NC_000007.13:g.50595839A>G , CM000669.1:g.50595839A>G GRCh37
NC_000007.12:g.50563333A>G NCBI36
NG_008742.1:g.42316T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001082971.2:c.710T>C (DDC) MANE Select NP_001076440.2:p.Phe237Ser
ENST00000444124.7:c.710T>C (DDC) MANE Select ENSP00000403644.2:p.Phe237Ser
NM_000790.3:c.710T>C (DDC) NP_000781.1:p.Phe237Ser
NM_000790.4:c.710T>C (DDC) NP_000781.2:p.Phe237Ser
NM_001082971.1:c.710T>C (DDC) NP_001076440.1:p.Phe237Ser
NM_001242886.1:c.596T>C (DDC) NP_001229815.1:p.Phe199Ser
NM_001242886.2:c.596T>C (DDC) NP_001229815.2:p.Phe199Ser
NM_001242887.1:c.570+1067T>C (DDC) NP_001229816.1:n.570+1067T>C
NM_001242887.2:c.570+1067T>C (DDC) NP_001229816.2:n.570+1067T>C
NM_001242888.1:c.476T>C (DDC) NP_001229817.1:p.Phe159Ser
NM_001242888.2:c.476T>C (DDC) NP_001229817.2:p.Phe159Ser
NM_001242889.1:c.435+9719T>C (DDC) NP_001229818.1:n.435+9719T>C
NM_001242889.2:c.435+9719T>C (DDC) NP_001229818.2:n.435+9719T>C
NM_001242890.1:c.710T>C (DDC) NP_001229819.1:p.Phe237Ser
NM_001242890.2:c.710T>C (DDC) NP_001229819.2:p.Phe237Ser
ENST00000357936.9:c.710T>C (DDC) ENSP00000350616.5:p.Phe237Ser
ENST00000380984.4:c.710T>C (DDC) ENSP00000370371.4:p.Phe237Ser
ENST00000426377.5:c.476T>C (DDC) ENSP00000395069.1:p.Phe159Ser
ENST00000430300.5:c.352T>C (DDC)
ENST00000431062.5:c.435+9719T>C (DDC) ENSP00000399184.1:n.435+9719T>C
ENST00000444124.6:c.710T>C (DDC) ENSP00000403644.2:p.Phe237Ser
ENST00000444733.5:c.596T>C (DDC) ENSP00000393724.1:p.Phe199Ser
ENST00000489162.1:n.509T>C (DDC)
ENST00000613602.3:c.-11+14377T>C (FIGNL1) ENSP00000481751.1:n.-11+14377T>C
ENST00000615193.4:c.435+9719T>C (DDC) ENSP00000484104.1:n.435+9719T>C
ENST00000617822.4:c.570+1067T>C (DDC) ENSP00000478385.1:n.570+1067T>C
ENST00000622873.4:c.596T>C (DDC) ENSP00000479110.1:p.Phe199Ser
XM_005271745.3:c.596T>C (DDC) XP_005271802.1:p.Phe199Ser
XM_005271745.4:c.596T>C (DDC) XP_005271802.1:p.Phe199Ser
XM_011515161.1:c.359T>C (DDC) XP_011513463.1:p.Phe120Ser
XM_011515161.2:c.653T>C (DDC) XP_011513463.2:p.Phe218Ser