Canonical Allele Identifier: CA2392518474

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138564G= , CM000683.2:g.46138564G=	GRCh38
NC_000021.8:g.47558478G= , CM000683.1:g.47558478G=	GRCh37
NC_000021.7:g.46382906G=	NCBI36
NG_016191.1:g.22004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-78C=	ENSP00000507070.1:n.-78C=
ENST00000494498.2:c.121C=	ENSP00000507847.1:p.Pro41=
ENST00000397746.8:c.1387C= MANE Select	ENSP00000380854.3:p.Pro463=
ENST00000291670.9:c.1387C=	ENSP00000291670.5:p.Pro463=
ENST00000397743.1:c.1343C=	ENSP00000380851.1:p.Ala448=
ENST00000397746.7:c.1387C=	ENSP00000380854.3:p.Pro463=
ENST00000397748.5:c.1387C=	ENSP00000380856.1:p.Pro463=
ENST00000446405.5:c.9C=
ENST00000460011.5:n.716C=
ENST00000488577.1:n.413C=
ENST00000494498.1:n.688C=
ENST00000498355.6:n.1456C=
NM_006657.2:c.1387C=	NP_006648.1:p.Pro463=
NM_206965.1:c.1387C=	NP_996848.1:p.Pro463=
XM_006723961.2:c.1636C=	XP_006724024.2:p.Pro546=
XM_006723962.2:c.1636C=	XP_006724025.2:p.Pro546=
XM_011529434.1:c.1636C=	XP_011527736.1:p.Pro546=
XM_011529435.1:c.1507C=	XP_011527737.1:p.Pro503=
XM_011529436.1:c.1636C=	XP_011527738.1:p.Pro546=
XM_011529437.1:c.1636C=	XP_011527739.1:p.Pro546=
XM_011529438.1:c.1507C=	XP_011527740.1:p.Pro503=
XM_011529439.1:c.1123C=	XP_011527741.1:p.Pro375=
XR_937433.1:n.1819C=
NM_001320412.1:c.1387C=	NP_001307341.1:p.Pro463=
XM_006723961.4:c.1636C=	XP_006724024.2:p.Pro546=
XM_006723962.4:c.1636C=	XP_006724025.2:p.Pro546=
XM_011529434.3:c.1636C=	XP_011527736.1:p.Pro546=
XM_011529435.3:c.1507C=	XP_011527737.1:p.Pro503=
XM_011529436.3:c.1636C=	XP_011527738.1:p.Pro546=
XM_011529437.3:c.1636C=	XP_011527739.1:p.Pro546=
XM_011529439.2:c.1123C=	XP_011527741.1:p.Pro375=
XR_937433.3:n.1853C=
NM_206965.2:c.1387C= MANE Select	NP_996848.1:p.Pro463=
NM_001320412.2:c.1387C=	NP_001307341.1:p.Pro463=
NM_006657.3:c.1387C=	NP_006648.1:p.Pro463=