Canonical Allele Identifier: CA367533540

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50470144A>C , CM000669.2:g.50470144A>C GRCh38
NC_000007.13:g.50537842A>C , CM000669.1:g.50537842A>C GRCh37
NC_000007.12:g.50505336A>C NCBI36
NG_008742.1:g.100313T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.1069T>G (DDC) MANE Select ENSP00000403644.2:p.Phe357Val
ENST00000357936.9:c.1069T>G (DDC) ENSP00000350616.5:p.Phe357Val
ENST00000426377.5:c.835T>G (DDC) ENSP00000395069.1:p.Phe279Val
ENST00000430300.5:c.711T>G (DDC)
ENST00000431062.5:c.790T>G (DDC) ENSP00000399184.1:p.Phe264Val
ENST00000444124.6:c.1069T>G (DDC) ENSP00000403644.2:p.Phe357Val
ENST00000444733.5:c.*170T>G (DDC) ENSP00000393724.1:n.*170T>G
ENST00000494914.1:n.225T>G (DDC)
ENST00000613602.3:c.-10-22847T>G (FIGNL1) ENSP00000481751.1:n.-10-22847T>G
ENST00000615193.4:c.790T>G (DDC) ENSP00000484104.1:p.Phe264Val
ENST00000617822.4:c.925T>G (DDC) ENSP00000478385.1:p.Phe309Val
ENST00000622873.4:c.955T>G (DDC) ENSP00000479110.1:p.Phe319Val
NM_000790.3:c.1069T>G (DDC) NP_000781.1:p.Phe357Val
NM_001082971.1:c.1069T>G (DDC) NP_001076440.1:p.Phe357Val
NM_001242886.1:c.955T>G (DDC) NP_001229815.1:p.Phe319Val
NM_001242887.1:c.925T>G (DDC) NP_001229816.1:p.Phe309Val
NM_001242888.1:c.835T>G (DDC) NP_001229817.1:p.Phe279Val
NM_001242889.1:c.790T>G (DDC) NP_001229818.1:p.Phe264Val
XM_005271745.3:c.955T>G (DDC) XP_005271802.1:p.Phe319Val
XM_011515161.1:c.718T>G (DDC) XP_011513463.1:p.Phe240Val
XM_005271745.4:c.955T>G (DDC) XP_005271802.1:p.Phe319Val
XM_011515161.2:c.1012T>G (DDC) XP_011513463.2:p.Phe338Val
NM_001082971.2:c.1069T>G (DDC) MANE Select NP_001076440.2:p.Phe357Val
NM_000790.4:c.1069T>G (DDC) NP_000781.2:p.Phe357Val
NM_001242888.2:c.835T>G (DDC) NP_001229817.2:p.Phe279Val
NM_001242886.2:c.955T>G (DDC) NP_001229815.2:p.Phe319Val
NM_001242887.2:c.925T>G (DDC) NP_001229816.2:p.Phe309Val
NM_001242889.2:c.790T>G (DDC) NP_001229818.2:p.Phe264Val