Canonical Allele Identifier: CA2392525836

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46150132T= , CM000683.2:g.46150132T=	GRCh38
NC_000021.8:g.47570046T= , CM000683.1:g.47570046T=	GRCh37
NC_000021.7:g.46394474T=	NCBI36
NG_016191.1:g.10436A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397746.8:c.893A= MANE Select	ENSP00000380854.3:p.Gln298=
ENST00000291670.9:c.893A=	ENSP00000291670.5:p.Gln298=
ENST00000397743.1:c.893A=	ENSP00000380851.1:p.Gln298=
ENST00000397746.7:c.893A=	ENSP00000380854.3:p.Gln298=
ENST00000397748.5:c.893A=	ENSP00000380856.1:p.Gln298=
ENST00000498355.6:n.962A=
NM_006657.2:c.893A=	NP_006648.1:p.Gln298=
NM_206965.1:c.893A=	NP_996848.1:p.Gln298=
XM_006723961.2:c.1013A=	XP_006724024.2:p.Gln338=
XM_006723962.2:c.1013A=	XP_006724025.2:p.Gln338=
XM_011529434.1:c.1013A=	XP_011527736.1:p.Gln338=
XM_011529435.1:c.1013A=	XP_011527737.1:p.Gln338=
XM_011529436.1:c.1013A=	XP_011527738.1:p.Gln338=
XM_011529437.1:c.1013A=	XP_011527739.1:p.Gln338=
XM_011529438.1:c.1013A=	XP_011527740.1:p.Gln338=
XM_011529439.1:c.500A=	XP_011527741.1:p.Gln167=
XM_011529440.1:c.1013A=	XP_011527742.1:p.Gln338=
XR_937433.1:n.1196A=
NM_001320412.1:c.893A=	NP_001307341.1:p.Gln298=
XM_006723961.4:c.1013A=	XP_006724024.2:p.Gln338=
XM_006723962.4:c.1013A=	XP_006724025.2:p.Gln338=
XM_011529434.3:c.1013A=	XP_011527736.1:p.Gln338=
XM_011529435.3:c.1013A=	XP_011527737.1:p.Gln338=
XM_011529436.3:c.1013A=	XP_011527738.1:p.Gln338=
XM_011529437.3:c.1013A=	XP_011527739.1:p.Gln338=
XM_011529439.2:c.500A=	XP_011527741.1:p.Gln167=
XM_011529440.3:c.1013A=	XP_011527742.1:p.Gln338=
XR_937433.3:n.1230A=
NM_206965.2:c.893A= MANE Select	NP_996848.1:p.Gln298=
NM_001320412.2:c.893A=	NP_001307341.1:p.Gln298=
NM_006657.3:c.893A=	NP_006648.1:p.Gln298=