Canonical Allele Identifier: CA1706649289

Gene: DDC FIGNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50529369_50529371delinsAAT , CM000669.2:g.50529369_50529371delinsAAT	GRCh38
NC_000007.13:g.50597067_50597069delinsAAT , CM000669.1:g.50597067_50597069delinsAAT	GRCh37
NC_000007.12:g.50564561_50564563delinsAAT	NCBI36
NG_008742.1:g.41086_41088delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444124.7:c.436-29_436-27delinsATT (DDC) MANE Select	ENSP00000403644.2:n.436-29_436-27delinsATT
ENST00000357936.9:c.436-29_436-27delinsATT (DDC)	ENSP00000350616.5:n.436-29_436-27delinsATT
ENST00000380984.4:c.436-29_436-27delinsATT (DDC)	ENSP00000370371.4:n.436-29_436-27delinsATT
ENST00000426377.5:c.202-29_202-27delinsATT (DDC)	ENSP00000395069.1:n.202-29_202-27delinsATT
ENST00000430300.5:c.213-1091_213-1089delinsATT (DDC)
ENST00000431062.5:c.435+8489_435+8491delinsATT (DDC)	ENSP00000399184.1:n.435+8489_435+8491delinsATT
ENST00000444124.6:c.436-29_436-27delinsATT (DDC)	ENSP00000403644.2:n.436-29_436-27delinsATT
ENST00000444733.5:c.322-29_322-27delinsATT (DDC)	ENSP00000393724.1:n.322-29_322-27delinsATT
ENST00000489162.1:n.235-29_235-27delinsATT (DDC)
ENST00000613602.3:c.-11+13147_-11+13149delinsATT (FIGNL1)	ENSP00000481751.1:n.-11+13147_-11+13149delinsATT
ENST00000615193.4:c.435+8489_435+8491delinsATT (DDC)	ENSP00000484104.1:n.435+8489_435+8491delinsATT
ENST00000617822.4:c.436-29_436-27delinsATT (DDC)	ENSP00000478385.1:n.436-29_436-27delinsATT
ENST00000622873.4:c.322-29_322-27delinsATT (DDC)	ENSP00000479110.1:n.322-29_322-27delinsATT
NM_000790.3:c.436-29_436-27delinsATT (DDC)	NP_000781.1:n.436-29_436-27delinsATT
NM_001082971.1:c.436-29_436-27delinsATT (DDC)	NP_001076440.1:n.436-29_436-27delinsATT
NM_001242886.1:c.322-29_322-27delinsATT (DDC)	NP_001229815.1:n.322-29_322-27delinsATT
NM_001242887.1:c.436-29_436-27delinsATT (DDC)	NP_001229816.1:n.436-29_436-27delinsATT
NM_001242888.1:c.202-29_202-27delinsATT (DDC)	NP_001229817.1:n.202-29_202-27delinsATT
NM_001242889.1:c.435+8489_435+8491delinsATT (DDC)	NP_001229818.1:n.435+8489_435+8491delinsATT
NM_001242890.1:c.436-29_436-27delinsATT (DDC)	NP_001229819.1:n.436-29_436-27delinsATT
XM_005271745.3:c.322-29_322-27delinsATT (DDC)	XP_005271802.1:n.322-29_322-27delinsATT
XM_011515161.1:c.85-29_85-27delinsATT (DDC)	XP_011513463.1:n.85-29_85-27delinsATT
XM_005271745.4:c.322-29_322-27delinsATT (DDC)	XP_005271802.1:n.322-29_322-27delinsATT
XM_011515161.2:c.379-29_379-27delinsATT (DDC)	XP_011513463.2:n.379-29_379-27delinsATT
NM_001082971.2:c.436-29_436-27delinsATT (DDC) MANE Select	NP_001076440.2:n.436-29_436-27delinsATT
NM_000790.4:c.436-29_436-27delinsATT (DDC)	NP_000781.2:n.436-29_436-27delinsATT
NM_001242888.2:c.202-29_202-27delinsATT (DDC)	NP_001229817.2:n.202-29_202-27delinsATT
NM_001242890.2:c.436-29_436-27delinsATT (DDC)	NP_001229819.2:n.436-29_436-27delinsATT
NM_001242886.2:c.322-29_322-27delinsATT (DDC)	NP_001229815.2:n.322-29_322-27delinsATT
NM_001242887.2:c.436-29_436-27delinsATT (DDC)	NP_001229816.2:n.436-29_436-27delinsATT
NM_001242889.2:c.435+8489_435+8491delinsATT (DDC)	NP_001229818.2:n.435+8489_435+8491delinsATT