Canonical Allele Identifier: CA2839173196

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138643dup , CM000683.2:g.46138643dup	GRCh38
NC_000021.8:g.47558557dup , CM000683.1:g.47558557dup	GRCh37
NC_000021.7:g.46382985dup	NCBI36
NG_016191.1:g.21925dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-157dup	ENSP00000507070.1:n.-157dup
ENST00000494498.2:c.42dup	ENSP00000507847.1:p.Thr15HisfsTer?
ENST00000397746.8:c.1308dup MANE Select	ENSP00000380854.3:p.Thr437HisfsTer?
ENST00000291670.9:c.1308dup	ENSP00000291670.5:p.Thr437HisfsTer?
ENST00000397743.1:c.1264dup	ENSP00000380851.1:p.His422ProfsTer9
ENST00000397746.7:c.1308dup	ENSP00000380854.3:p.Thr437HisfsTer?
ENST00000397748.5:c.1308dup	ENSP00000380856.1:p.Thr437HisfsTer?
ENST00000460011.5:n.637dup
ENST00000488577.1:n.334dup
ENST00000494498.1:n.609dup
ENST00000498355.6:n.1377dup
NM_006657.2:c.1308dup	NP_006648.1:p.Thr437HisfsTer?
NM_206965.1:c.1308dup	NP_996848.1:p.Thr437HisfsTer?
XM_006723961.2:c.1557dup	XP_006724024.2:p.Thr520HisfsTer?
XM_006723962.2:c.1557dup	XP_006724025.2:p.Thr520HisfsTer?
XM_011529434.1:c.1557dup	XP_011527736.1:p.Thr520HisfsTer?
XM_011529435.1:c.1428dup	XP_011527737.1:p.Thr477HisfsTer?
XM_011529436.1:c.1557dup	XP_011527738.1:p.Thr520HisfsTer?
XM_011529437.1:c.1557dup	XP_011527739.1:p.Thr520HisfsTer?
XM_011529438.1:c.1428dup	XP_011527740.1:p.Thr477HisfsTer?
XM_011529439.1:c.1044dup	XP_011527741.1:p.Thr349HisfsTer?
XR_937433.1:n.1740dup
NM_001320412.1:c.1308dup	NP_001307341.1:p.Thr437HisfsTer?
XM_006723961.4:c.1557dup	XP_006724024.2:p.Thr520HisfsTer?
XM_006723962.4:c.1557dup	XP_006724025.2:p.Thr520HisfsTer?
XM_011529434.3:c.1557dup	XP_011527736.1:p.Thr520HisfsTer?
XM_011529435.3:c.1428dup	XP_011527737.1:p.Thr477HisfsTer?
XM_011529436.3:c.1557dup	XP_011527738.1:p.Thr520HisfsTer?
XM_011529437.3:c.1557dup	XP_011527739.1:p.Thr520HisfsTer?
XM_011529439.2:c.1044dup	XP_011527741.1:p.Thr349HisfsTer?
XR_937433.3:n.1774dup
NM_206965.2:c.1308dup MANE Select	NP_996848.1:p.Thr437HisfsTer?
NM_001320412.2:c.1308dup	NP_001307341.1:p.Thr437HisfsTer?
NM_006657.3:c.1308dup	NP_006648.1:p.Thr437HisfsTer?