Canonical Allele Identifier: CA2392518484

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138575_46138578delinsGCCA , CM000683.2:g.46138575_46138578delinsGCCA	GRCh38
NC_000021.8:g.47558489_47558492delinsGCCA , CM000683.1:g.47558489_47558492delinsGCCA	GRCh37
NC_000021.7:g.46382917_46382920delinsGCCA	NCBI36
NG_016191.1:g.21990_21993delinsTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-92_-89delinsTGGC	ENSP00000507070.1:n.-92_-89delinsTGGC
ENST00000494498.2:c.107_110delinsTGGC	ENSP00000507847.1:p.Val36=
ENST00000397746.8:c.1373_1376delinsTGGC MANE Select	ENSP00000380854.3:p.Val458=
ENST00000291670.9:c.1373_1376delinsTGGC	ENSP00000291670.5:p.Val458=
ENST00000397743.1:c.1329_1332delinsTGGC	ENSP00000380851.1:p.Gly443=
ENST00000397746.7:c.1373_1376delinsTGGC	ENSP00000380854.3:p.Val458=
ENST00000397748.5:c.1373_1376delinsTGGC	ENSP00000380856.1:p.Val458=
ENST00000460011.5:n.702_705delinsTGGC
ENST00000488577.1:n.399_402delinsTGGC
ENST00000494498.1:n.674_677delinsTGGC
ENST00000498355.6:n.1442_1445delinsTGGC
NM_006657.2:c.1373_1376delinsTGGC	NP_006648.1:p.Val458=
NM_206965.1:c.1373_1376delinsTGGC	NP_996848.1:p.Val458=
XM_006723961.2:c.1622_1625delinsTGGC	XP_006724024.2:p.Val541=
XM_006723962.2:c.1622_1625delinsTGGC	XP_006724025.2:p.Val541=
XM_011529434.1:c.1622_1625delinsTGGC	XP_011527736.1:p.Val541=
XM_011529435.1:c.1493_1496delinsTGGC	XP_011527737.1:p.Val498=
XM_011529436.1:c.1622_1625delinsTGGC	XP_011527738.1:p.Val541=
XM_011529437.1:c.1622_1625delinsTGGC	XP_011527739.1:p.Val541=
XM_011529438.1:c.1493_1496delinsTGGC	XP_011527740.1:p.Val498=
XM_011529439.1:c.1109_1112delinsTGGC	XP_011527741.1:p.Val370=
XR_937433.1:n.1805_1808delinsTGGC
NM_001320412.1:c.1373_1376delinsTGGC	NP_001307341.1:p.Val458=
XM_006723961.4:c.1622_1625delinsTGGC	XP_006724024.2:p.Val541=
XM_006723962.4:c.1622_1625delinsTGGC	XP_006724025.2:p.Val541=
XM_011529434.3:c.1622_1625delinsTGGC	XP_011527736.1:p.Val541=
XM_011529435.3:c.1493_1496delinsTGGC	XP_011527737.1:p.Val498=
XM_011529436.3:c.1622_1625delinsTGGC	XP_011527738.1:p.Val541=
XM_011529437.3:c.1622_1625delinsTGGC	XP_011527739.1:p.Val541=
XM_011529439.2:c.1109_1112delinsTGGC	XP_011527741.1:p.Val370=
XR_937433.3:n.1839_1842delinsTGGC
NM_206965.2:c.1373_1376delinsTGGC MANE Select	NP_996848.1:p.Val458=
NM_001320412.2:c.1373_1376delinsTGGC	NP_001307341.1:p.Val458=
NM_006657.3:c.1373_1376delinsTGGC	NP_006648.1:p.Val458=