Canonical Allele Identifier: CA2838467104

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50476617dup , CM000669.2:g.50476617dup	GRCh38
NC_000007.13:g.50544315dup , CM000669.1:g.50544315dup	GRCh37
NC_000007.12:g.50511809dup	NCBI36
NG_008742.1:g.93842dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.1041+9dup (DDC) MANE Select	ENSP00000403644.2:n.1041+9dup
ENST00000357936.9:c.1041+9dup (DDC)	ENSP00000350616.5:n.1041+9dup
ENST00000426377.5:c.807+9dup (DDC)	ENSP00000395069.1:n.807+9dup
ENST00000430300.5:c.683+9dup (DDC)
ENST00000431062.5:c.762+9dup (DDC)	ENSP00000399184.1:n.762+9dup
ENST00000444124.6:c.1041+9dup (DDC)	ENSP00000403644.2:n.1041+9dup
ENST00000444733.5:c.*142+9dup (DDC)	ENSP00000393724.1:n.*142+9dup
ENST00000494914.1:n.197+9dup (DDC)
ENST00000613602.3:c.-10-29318dup (FIGNL1)	ENSP00000481751.1:n.-10-29318dup
ENST00000615193.4:c.762+9dup (DDC)	ENSP00000484104.1:n.762+9dup
ENST00000617822.4:c.897+9dup (DDC)	ENSP00000478385.1:n.897+9dup
ENST00000622873.4:c.927+9dup (DDC)	ENSP00000479110.1:n.927+9dup
NM_000790.3:c.1041+9dup (DDC)	NP_000781.1:n.1041+9dup
NM_001082971.1:c.1041+9dup (DDC)	NP_001076440.1:n.1041+9dup
NM_001242886.1:c.927+9dup (DDC)	NP_001229815.1:n.927+9dup
NM_001242887.1:c.897+9dup (DDC)	NP_001229816.1:n.897+9dup
NM_001242888.1:c.807+9dup (DDC)	NP_001229817.1:n.807+9dup
NM_001242889.1:c.762+9dup (DDC)	NP_001229818.1:n.762+9dup
XM_005271745.3:c.927+9dup (DDC)	XP_005271802.1:n.927+9dup
XM_011515161.1:c.690+9dup (DDC)	XP_011513463.1:n.690+9dup
XM_005271745.4:c.927+9dup (DDC)	XP_005271802.1:n.927+9dup
XM_011515161.2:c.984+9dup (DDC)	XP_011513463.2:n.984+9dup
NM_001082971.2:c.1041+9dup (DDC) MANE Select	NP_001076440.2:n.1041+9dup
NM_000790.4:c.1041+9dup (DDC)	NP_000781.2:n.1041+9dup
NM_001242888.2:c.807+9dup (DDC)	NP_001229817.2:n.807+9dup
NM_001242886.2:c.927+9dup (DDC)	NP_001229815.2:n.927+9dup
NM_001242887.2:c.897+9dup (DDC)	NP_001229816.2:n.897+9dup
NM_001242889.2:c.762+9dup (DDC)	NP_001229818.2:n.762+9dup