Canonical Allele Identifier: CA2654984237

Gene: FTCD

Linked Data

• gnomAD v4: 21-46150036-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46150040del , CM000683.2:g.46150040del	GRCh38
NC_000021.8:g.47569954del , CM000683.1:g.47569954del	GRCh37
NC_000021.7:g.46394382del	NCBI36
NG_016191.1:g.10531del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397746.8:c.906+82del MANE Select	ENSP00000380854.3:n.906+82del
ENST00000291670.9:c.906+82del	ENSP00000291670.5:n.906+82del
ENST00000397743.1:c.906+82del	ENSP00000380851.1:n.906+82del
ENST00000397746.7:c.906+82del	ENSP00000380854.3:n.906+82del
ENST00000397748.5:c.906+82del	ENSP00000380856.1:n.906+82del
ENST00000498355.6:n.975+82del
NM_006657.2:c.906+82del	NP_006648.1:n.906+82del
NM_206965.1:c.906+82del	NP_996848.1:n.906+82del
XM_006723961.2:c.1026+82del	XP_006724024.2:n.1026+82del
XM_006723962.2:c.1026+82del	XP_006724025.2:n.1026+82del
XM_011529434.1:c.1026+82del	XP_011527736.1:n.1026+82del
XM_011529435.1:c.1026+82del	XP_011527737.1:n.1026+82del
XM_011529436.1:c.1026+82del	XP_011527738.1:n.1026+82del
XM_011529437.1:c.1026+82del	XP_011527739.1:n.1026+82del
XM_011529438.1:c.1026+82del	XP_011527740.1:n.1026+82del
XM_011529439.1:c.513+82del	XP_011527741.1:n.513+82del
XM_011529440.1:c.1026+82del	XP_011527742.1:n.1026+82del
XR_937433.1:n.1209+82del
NM_001320412.1:c.906+82del	NP_001307341.1:n.906+82del
XM_006723961.4:c.1026+82del	XP_006724024.2:n.1026+82del
XM_006723962.4:c.1026+82del	XP_006724025.2:n.1026+82del
XM_011529434.3:c.1026+82del	XP_011527736.1:n.1026+82del
XM_011529435.3:c.1026+82del	XP_011527737.1:n.1026+82del
XM_011529436.3:c.1026+82del	XP_011527738.1:n.1026+82del
XM_011529437.3:c.1026+82del	XP_011527739.1:n.1026+82del
XM_011529439.2:c.513+82del	XP_011527741.1:n.513+82del
XM_011529440.3:c.1026+82del	XP_011527742.1:n.1026+82del
XR_937433.3:n.1243+82del
NM_206965.2:c.906+82del MANE Select	NP_996848.1:n.906+82del
NM_001320412.2:c.906+82del	NP_001307341.1:n.906+82del
NM_006657.3:c.906+82del	NP_006648.1:n.906+82del