Canonical Allele Identifier: CA2026154274

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50529209_50529210insATCG , CM000669.2:g.50529209_50529210insATCG	GRCh38
NC_000007.13:g.50596907_50596908insATCG , CM000669.1:g.50596907_50596908insATCG	GRCh37
NC_000007.12:g.50564401_50564402insATCG	NCBI36
NG_008742.1:g.41247_41248insCGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.568_569insCGAT (DDC) MANE Select	ENSP00000403644.2:p.Gln190ProfsTer?
ENST00000357936.9:c.568_569insCGAT (DDC)	ENSP00000350616.5:p.Gln190ProfsTer?
ENST00000380984.4:c.568_569insCGAT (DDC)	ENSP00000370371.4:p.Gln190ProfsTer?
ENST00000426377.5:c.334_335insCGAT (DDC)	ENSP00000395069.1:p.Gln112ProfsTer?
ENST00000430300.5:c.213-930_213-929insCGAT (DDC)
ENST00000431062.5:c.435+8650_435+8651insCGAT (DDC)	ENSP00000399184.1:n.435+8650_435+8651insCGAT
ENST00000444124.6:c.568_569insCGAT (DDC)	ENSP00000403644.2:p.Gln190ProfsTer?
ENST00000444733.5:c.454_455insCGAT (DDC)	ENSP00000393724.1:p.Gln152ProfsTer?
ENST00000489162.1:n.367_368insCGAT (DDC)
ENST00000613602.3:c.-11+13308_-11+13309insCGAT (FIGNL1)	ENSP00000481751.1:n.-11+13308_-11+13309insCGAT
ENST00000615193.4:c.435+8650_435+8651insCGAT (DDC)	ENSP00000484104.1:n.435+8650_435+8651insCGAT
ENST00000617822.4:c.568_569insCGAT (DDC)	ENSP00000478385.1:p.Gln190ProfsTer16
ENST00000622873.4:c.454_455insCGAT (DDC)	ENSP00000479110.1:p.Gln152ProfsTer?
NM_000790.3:c.568_569insCGAT (DDC)	NP_000781.1:p.Gln190ProfsTer?
NM_001082971.1:c.568_569insCGAT (DDC)	NP_001076440.1:p.Gln190ProfsTer?
NM_001242886.1:c.454_455insCGAT (DDC)	NP_001229815.1:p.Gln152ProfsTer?
NM_001242887.1:c.568_569insCGAT (DDC)	NP_001229816.1:p.Gln190ProfsTer16
NM_001242888.1:c.334_335insCGAT (DDC)	NP_001229817.1:p.Gln112ProfsTer?
NM_001242889.1:c.435+8650_435+8651insCGAT (DDC)	NP_001229818.1:n.435+8650_435+8651insCGAT
NM_001242890.1:c.568_569insCGAT (DDC)	NP_001229819.1:p.Gln190ProfsTer?
XM_005271745.3:c.454_455insCGAT (DDC)	XP_005271802.1:p.Gln152ProfsTer?
XM_011515161.1:c.217_218insCGAT (DDC)	XP_011513463.1:p.Gln73ProfsTer?
XM_005271745.4:c.454_455insCGAT (DDC)	XP_005271802.1:p.Gln152ProfsTer?
XM_011515161.2:c.511_512insCGAT (DDC)	XP_011513463.2:p.Gln171ProfsTer?
NM_001082971.2:c.568_569insCGAT (DDC) MANE Select	NP_001076440.2:p.Gln190ProfsTer?
NM_000790.4:c.568_569insCGAT (DDC)	NP_000781.2:p.Gln190ProfsTer?
NM_001242888.2:c.334_335insCGAT (DDC)	NP_001229817.2:p.Gln112ProfsTer?
NM_001242890.2:c.568_569insCGAT (DDC)	NP_001229819.2:p.Gln190ProfsTer?
NM_001242886.2:c.454_455insCGAT (DDC)	NP_001229815.2:p.Gln152ProfsTer?
NM_001242887.2:c.568_569insCGAT (DDC)	NP_001229816.2:p.Gln190ProfsTer16
NM_001242889.2:c.435+8650_435+8651insCGAT (DDC)	NP_001229818.2:n.435+8650_435+8651insCGAT