Canonical Allele Identifier: CA2654976948

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138534-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138537del , CM000683.2:g.46138537del	GRCh38
NC_000021.8:g.47558451del , CM000683.1:g.47558451del	GRCh37
NC_000021.7:g.46382879del	NCBI36
NG_016191.1:g.22033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-49del	ENSP00000507070.1:n.-49del
ENST00000494498.2:c.150del	ENSP00000507847.1:p.Asn51ThrfsTer?
ENST00000397746.8:c.1416del MANE Select	ENSP00000380854.3:p.Asn473ThrfsTer?
ENST00000291670.9:c.1416del	ENSP00000291670.5:p.Asn473ThrfsTer?
ENST00000397743.1:c.1372del	ENSP00000380851.1:p.Glu458AsnfsTer?
ENST00000397746.7:c.1416del	ENSP00000380854.3:p.Asn473ThrfsTer?
ENST00000397748.5:c.1416del	ENSP00000380856.1:p.Asn473ThrfsTer?
ENST00000446405.5:c.38del
ENST00000460011.5:n.745del
ENST00000488577.1:n.442del
ENST00000494498.1:n.717del
ENST00000498355.6:n.1485del
NM_006657.2:c.1416del	NP_006648.1:p.Asn473ThrfsTer?
NM_206965.1:c.1416del	NP_996848.1:p.Asn473ThrfsTer?
XM_006723961.2:c.1665del	XP_006724024.2:p.Asn556ThrfsTer?
XM_006723962.2:c.1665del	XP_006724025.2:p.Asn556ThrfsTer?
XM_011529434.1:c.1665del	XP_011527736.1:p.Asn556ThrfsTer?
XM_011529435.1:c.1536del	XP_011527737.1:p.Asn513ThrfsTer?
XM_011529436.1:c.1665del	XP_011527738.1:p.Asn556ThrfsTer?
XM_011529437.1:c.1665del	XP_011527739.1:p.Asn556ThrfsTer?
XM_011529438.1:c.1536del	XP_011527740.1:p.Asn513ThrfsTer?
XM_011529439.1:c.1152del	XP_011527741.1:p.Asn385ThrfsTer?
XR_937433.1:n.1848del
NM_001320412.1:c.1416del	NP_001307341.1:p.Asn473ThrfsTer?
XM_006723961.4:c.1665del	XP_006724024.2:p.Asn556ThrfsTer?
XM_006723962.4:c.1665del	XP_006724025.2:p.Asn556ThrfsTer?
XM_011529434.3:c.1665del	XP_011527736.1:p.Asn556ThrfsTer?
XM_011529435.3:c.1536del	XP_011527737.1:p.Asn513ThrfsTer?
XM_011529436.3:c.1665del	XP_011527738.1:p.Asn556ThrfsTer?
XM_011529437.3:c.1665del	XP_011527739.1:p.Asn556ThrfsTer?
XM_011529439.2:c.1152del	XP_011527741.1:p.Asn385ThrfsTer?
XR_937433.3:n.1882del
NM_206965.2:c.1416del MANE Select	NP_996848.1:p.Asn473ThrfsTer?
NM_001320412.2:c.1416del	NP_001307341.1:p.Asn473ThrfsTer?
NM_006657.3:c.1416del	NP_006648.1:p.Asn473ThrfsTer?