Canonical Allele Identifier: CA2539909097

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50485316_50485317insAGAGA , CM000669.2:g.50485316_50485317insAGAGA	GRCh38
NC_000007.13:g.50553014_50553015insAGAGA , CM000669.1:g.50553014_50553015insAGAGA	GRCh37
NC_000007.12:g.50520508_50520509insAGAGA	NCBI36
NG_008742.1:g.85141_85142insCTCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000444124.7:c.945-5453_945-5452insCTCTT (DDC) MANE Select	ENSP00000403644.2:n.945-5453_945-5452insC...
ENST00000357936.9:c.945-5453_945-5452insCTCTT (DDC)	ENSP00000350616.5:n.945-5453_945-5452insC...
ENST00000426377.5:c.711-5453_711-5452insCTCTT (DDC)	ENSP00000395069.1:n.711-5453_711-5452insC...
ENST00000430300.5:c.587-5453_587-5452insCTCTT (DDC)
ENST00000431062.5:c.666-5453_666-5452insCTCTT (DDC)	ENSP00000399184.1:n.666-5453_666-5452insC...
ENST00000444124.6:c.945-5453_945-5452insCTCTT (DDC)	ENSP00000403644.2:n.945-5453_945-5452insC...
ENST00000444733.5:c.*46-5453_*46-5452insCTCTT (DDC)	ENSP00000393724.1:n.*46-5453_*46-5452insC...
ENST00000613602.3:c.-10-38019_-10-38018insCTCTT (FIGNL1)	ENSP00000481751.1:n.-10-38019_-10-38018in...
ENST00000615193.4:c.666-5453_666-5452insCTCTT (DDC)	ENSP00000484104.1:n.666-5453_666-5452insC...
ENST00000617822.4:c.801-5453_801-5452insCTCTT (DDC)	ENSP00000478385.1:n.801-5453_801-5452insC...
ENST00000622873.4:c.831-5453_831-5452insCTCTT (DDC)	ENSP00000479110.1:n.831-5453_831-5452insC...
NM_000790.3:c.945-5453_945-5452insCTCTT (DDC)	NP_000781.1:n.945-5453_945-5452insCTCTT
NM_001082971.1:c.945-5453_945-5452insCTCTT (DDC)	NP_001076440.1:n.945-5453_945-5452insCTCT...
NM_001242886.1:c.831-5453_831-5452insCTCTT (DDC)	NP_001229815.1:n.831-5453_831-5452insCTCT...
NM_001242887.1:c.801-5453_801-5452insCTCTT (DDC)	NP_001229816.1:n.801-5453_801-5452insCTCT...
NM_001242888.1:c.711-5453_711-5452insCTCTT (DDC)	NP_001229817.1:n.711-5453_711-5452insCTCT...
NM_001242889.1:c.666-5453_666-5452insCTCTT (DDC)	NP_001229818.1:n.666-5453_666-5452insCTCT...
XM_005271745.3:c.831-5453_831-5452insCTCTT (DDC)	XP_005271802.1:n.831-5453_831-5452insCTCT...
XM_011515161.1:c.594-5453_594-5452insCTCTT (DDC)	XP_011513463.1:n.594-5453_594-5452insCTCT...
XM_005271745.4:c.831-5453_831-5452insCTCTT (DDC)	XP_005271802.1:n.831-5453_831-5452insCTCT...
XM_011515161.2:c.888-5453_888-5452insCTCTT (DDC)	XP_011513463.2:n.888-5453_888-5452insCTCT...
NM_001082971.2:c.945-5453_945-5452insCTCTT (DDC) MANE Select	NP_001076440.2:n.945-5453_945-5452insCTCT...
NM_000790.4:c.945-5453_945-5452insCTCTT (DDC)	NP_000781.2:n.945-5453_945-5452insCTCTT
NM_001242888.2:c.711-5453_711-5452insCTCTT (DDC)	NP_001229817.2:n.711-5453_711-5452insCTCT...
NM_001242886.2:c.831-5453_831-5452insCTCTT (DDC)	NP_001229815.2:n.831-5453_831-5452insCTCT...
NM_001242887.2:c.801-5453_801-5452insCTCTT (DDC)	NP_001229816.2:n.801-5453_801-5452insCTCT...
NM_001242889.2:c.666-5453_666-5452insCTCTT (DDC)	NP_001229818.2:n.666-5453_666-5452insCTCT...