Canonical Allele Identifier: CA2392518522

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138633G= , CM000683.2:g.46138633G=	GRCh38
NC_000021.8:g.47558547G= , CM000683.1:g.47558547G=	GRCh37
NC_000021.7:g.46382975G=	NCBI36
NG_016191.1:g.21935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-147C=	ENSP00000507070.1:n.-147C=
ENST00000494498.2:c.52C=	ENSP00000507847.1:p.Leu18=
ENST00000397746.8:c.1318C= MANE Select	ENSP00000380854.3:p.Leu440=
ENST00000291670.9:c.1318C=	ENSP00000291670.5:p.Leu440=
ENST00000397743.1:c.1274C=	ENSP00000380851.1:p.Pro425=
ENST00000397746.7:c.1318C=	ENSP00000380854.3:p.Leu440=
ENST00000397748.5:c.1318C=	ENSP00000380856.1:p.Leu440=
ENST00000460011.5:n.647C=
ENST00000488577.1:n.344C=
ENST00000494498.1:n.619C=
ENST00000498355.6:n.1387C=
NM_006657.2:c.1318C=	NP_006648.1:p.Leu440=
NM_206965.1:c.1318C=	NP_996848.1:p.Leu440=
XM_006723961.2:c.1567C=	XP_006724024.2:p.Leu523=
XM_006723962.2:c.1567C=	XP_006724025.2:p.Leu523=
XM_011529434.1:c.1567C=	XP_011527736.1:p.Leu523=
XM_011529435.1:c.1438C=	XP_011527737.1:p.Leu480=
XM_011529436.1:c.1567C=	XP_011527738.1:p.Leu523=
XM_011529437.1:c.1567C=	XP_011527739.1:p.Leu523=
XM_011529438.1:c.1438C=	XP_011527740.1:p.Leu480=
XM_011529439.1:c.1054C=	XP_011527741.1:p.Leu352=
XR_937433.1:n.1750C=
NM_001320412.1:c.1318C=	NP_001307341.1:p.Leu440=
XM_006723961.4:c.1567C=	XP_006724024.2:p.Leu523=
XM_006723962.4:c.1567C=	XP_006724025.2:p.Leu523=
XM_011529434.3:c.1567C=	XP_011527736.1:p.Leu523=
XM_011529435.3:c.1438C=	XP_011527737.1:p.Leu480=
XM_011529436.3:c.1567C=	XP_011527738.1:p.Leu523=
XM_011529437.3:c.1567C=	XP_011527739.1:p.Leu523=
XM_011529439.2:c.1054C=	XP_011527741.1:p.Leu352=
XR_937433.3:n.1784C=
NM_206965.2:c.1318C= MANE Select	NP_996848.1:p.Leu440=
NM_001320412.2:c.1318C=	NP_001307341.1:p.Leu440=
NM_006657.3:c.1318C=	NP_006648.1:p.Leu440=