Canonical Allele Identifier: CA367533544

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000444124.7:c.1069T>A (DDC) MANE Select ENSP00000403644.2:p.Phe357Ile
ENST00000357936.9:c.1069T>A (DDC) ENSP00000350616.5:p.Phe357Ile
ENST00000426377.5:c.835T>A (DDC) ENSP00000395069.1:p.Phe279Ile
ENST00000430300.5:c.711T>A (DDC)
ENST00000431062.5:c.790T>A (DDC) ENSP00000399184.1:p.Phe264Ile
ENST00000444124.6:c.1069T>A (DDC) ENSP00000403644.2:p.Phe357Ile
ENST00000444733.5:c.*170T>A (DDC) ENSP00000393724.1:n.*170T>A
ENST00000494914.1:n.225T>A (DDC)
ENST00000613602.3:c.-10-22847T>A (FIGNL1) ENSP00000481751.1:n.-10-22847T>A
ENST00000615193.4:c.790T>A (DDC) ENSP00000484104.1:p.Phe264Ile
ENST00000617822.4:c.925T>A (DDC) ENSP00000478385.1:p.Phe309Ile
ENST00000622873.4:c.955T>A (DDC) ENSP00000479110.1:p.Phe319Ile
NM_000790.3:c.1069T>A (DDC) NP_000781.1:p.Phe357Ile
NM_001082971.1:c.1069T>A (DDC) NP_001076440.1:p.Phe357Ile
NM_001242886.1:c.955T>A (DDC) NP_001229815.1:p.Phe319Ile
NM_001242887.1:c.925T>A (DDC) NP_001229816.1:p.Phe309Ile
NM_001242888.1:c.835T>A (DDC) NP_001229817.1:p.Phe279Ile
NM_001242889.1:c.790T>A (DDC) NP_001229818.1:p.Phe264Ile
XM_005271745.3:c.955T>A (DDC) XP_005271802.1:p.Phe319Ile
XM_011515161.1:c.718T>A (DDC) XP_011513463.1:p.Phe240Ile
XM_005271745.4:c.955T>A (DDC) XP_005271802.1:p.Phe319Ile
XM_011515161.2:c.1012T>A (DDC) XP_011513463.2:p.Phe338Ile
NM_001082971.2:c.1069T>A (DDC) MANE Select NP_001076440.2:p.Phe357Ile
NM_000790.4:c.1069T>A (DDC) NP_000781.2:p.Phe357Ile
NM_001242888.2:c.835T>A (DDC) NP_001229817.2:p.Phe279Ile
NM_001242886.2:c.955T>A (DDC) NP_001229815.2:p.Phe319Ile
NM_001242887.2:c.925T>A (DDC) NP_001229816.2:p.Phe309Ile
NM_001242889.2:c.790T>A (DDC) NP_001229818.2:p.Phe264Ile