Canonical Allele Identifier: CA1706635417

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50495382C= , CM000669.2:g.50495382C=	GRCh38
NC_000007.13:g.50563080C= , CM000669.1:g.50563080C=	GRCh37
NC_000007.12:g.50530574C=	NCBI36
NG_008742.1:g.75075G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.912G= (DDC) MANE Select	ENSP00000403644.2:p.Trp304=
ENST00000357936.9:c.912G= (DDC)	ENSP00000350616.5:p.Trp304=
ENST00000380984.4:c.912G= (DDC)	ENSP00000370371.4:p.Trp304=
ENST00000426377.5:c.678G= (DDC)	ENSP00000395069.1:p.Trp226=
ENST00000430300.5:c.554G= (DDC)
ENST00000431062.5:c.633G= (DDC)	ENSP00000399184.1:p.Trp211=
ENST00000444124.6:c.912G= (DDC)	ENSP00000403644.2:p.Trp304=
ENST00000444733.5:c.*13G= (DDC)	ENSP00000393724.1:n.*13G=
ENST00000613602.3:c.-11+47136G= (FIGNL1)	ENSP00000481751.1:n.-11+47136G=
ENST00000615193.4:c.633G= (DDC)	ENSP00000484104.1:p.Trp211=
ENST00000617822.4:c.768G= (DDC)	ENSP00000478385.1:p.Trp256=
ENST00000622873.4:c.798G= (DDC)	ENSP00000479110.1:p.Trp266=
NM_000790.3:c.912G= (DDC)	NP_000781.1:p.Trp304=
NM_001082971.1:c.912G= (DDC)	NP_001076440.1:p.Trp304=
NM_001242886.1:c.798G= (DDC)	NP_001229815.1:p.Trp266=
NM_001242887.1:c.768G= (DDC)	NP_001229816.1:p.Trp256=
NM_001242888.1:c.678G= (DDC)	NP_001229817.1:p.Trp226=
NM_001242889.1:c.633G= (DDC)	NP_001229818.1:p.Trp211=
NM_001242890.1:c.912G= (DDC)	NP_001229819.1:p.Trp304=
XM_005271745.3:c.798G= (DDC)	XP_005271802.1:p.Trp266=
XM_011515161.1:c.561G= (DDC)	XP_011513463.1:p.Trp187=
XM_005271745.4:c.798G= (DDC)	XP_005271802.1:p.Trp266=
XM_011515161.2:c.855G= (DDC)	XP_011513463.2:p.Trp285=
NM_001082971.2:c.912G= (DDC) MANE Select	NP_001076440.2:p.Trp304=
NM_000790.4:c.912G= (DDC)	NP_000781.2:p.Trp304=
NM_001242888.2:c.678G= (DDC)	NP_001229817.2:p.Trp226=
NM_001242890.2:c.912G= (DDC)	NP_001229819.2:p.Trp304=
NM_001242886.2:c.798G= (DDC)	NP_001229815.2:p.Trp266=
NM_001242887.2:c.768G= (DDC)	NP_001229816.2:p.Trp256=
NM_001242889.2:c.633G= (DDC)	NP_001229818.2:p.Trp211=