Canonical Allele Identifier: CA158225556

Gene: DDC FIGNL1

Linked Data

• dbSNP Id: rs35517528

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50476625dup , CM000669.2:g.50476625dup	GRCh38
NC_000007.13:g.50544323dup , CM000669.1:g.50544323dup	GRCh37
NC_000007.12:g.50511817dup	NCBI36
NG_008742.1:g.93834dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000444124.7:c.1041+1dup (DDC)
ENST00000357936.9:c.1041+1dup (DDC)
ENST00000426377.5:c.807+1dup (DDC)
ENST00000430300.5:c.683+1dup (DDC)
ENST00000431062.5:c.762+1dup (DDC)
ENST00000444124.6:c.1041+1dup (DDC)
ENST00000444733.5:c.*142+1dup (DDC)
ENST00000494914.1:n.197+1dup (DDC)
ENST00000613602.3:c.-10-29326dup (FIGNL1)	ENSP00000481751.1:n.-10-29326dup
ENST00000615193.4:c.762+1dup (DDC)
ENST00000617822.4:c.897+1dup (DDC)
ENST00000622873.4:c.927+1dup (DDC)
NM_000790.3:c.1041+1dup (DDC)
NM_001082971.1:c.1041+1dup (DDC)
NM_001242886.1:c.927+1dup (DDC)
NM_001242887.1:c.897+1dup (DDC)
NM_001242888.1:c.807+1dup (DDC)
NM_001242889.1:c.762+1dup (DDC)
XM_005271745.3:c.927+1dup (DDC)
XM_011515161.1:c.690+1dup (DDC)
XM_005271745.4:c.927+1dup (DDC)
XM_011515161.2:c.984+1dup (DDC)
NM_001082971.2:c.1041+1dup (DDC)
NM_000790.4:c.1041+1dup (DDC)
NM_001242888.2:c.807+1dup (DDC)
NM_001242886.2:c.927+1dup (DDC)
NM_001242887.2:c.897+1dup (DDC)
NM_001242889.2:c.762+1dup (DDC)