Canonical Allele Identifier: CA2654977148

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138631-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138632_46138633del , CM000683.2:g.46138632_46138633del	GRCh38
NC_000021.8:g.47558546_47558547del , CM000683.1:g.47558546_47558547del	GRCh37
NC_000021.7:g.46382974_46382975del	NCBI36
NG_016191.1:g.21935_21936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-147_-146del	ENSP00000507070.1:n.-147_-146del
ENST00000494498.2:c.52_53del	ENSP00000507847.1:p.Leu18ThrfsTer?
ENST00000397746.8:c.1318_1319del MANE Select	ENSP00000380854.3:p.Leu440ThrfsTer?
ENST00000291670.9:c.1318_1319del	ENSP00000291670.5:p.Leu440ThrfsTer?
ENST00000397743.1:c.1274_1275del	ENSP00000380851.1:p.Pro425HisfsTer5
ENST00000397746.7:c.1318_1319del	ENSP00000380854.3:p.Leu440ThrfsTer?
ENST00000397748.5:c.1318_1319del	ENSP00000380856.1:p.Leu440ThrfsTer?
ENST00000460011.5:n.647_648del
ENST00000488577.1:n.344_345del
ENST00000494498.1:n.619_620del
ENST00000498355.6:n.1387_1388del
NM_006657.2:c.1318_1319del	NP_006648.1:p.Leu440ThrfsTer?
NM_206965.1:c.1318_1319del	NP_996848.1:p.Leu440ThrfsTer?
XM_006723961.2:c.1567_1568del	XP_006724024.2:p.Leu523ThrfsTer?
XM_006723962.2:c.1567_1568del	XP_006724025.2:p.Leu523ThrfsTer?
XM_011529434.1:c.1567_1568del	XP_011527736.1:p.Leu523ThrfsTer?
XM_011529435.1:c.1438_1439del	XP_011527737.1:p.Leu480ThrfsTer?
XM_011529436.1:c.1567_1568del	XP_011527738.1:p.Leu523ThrfsTer?
XM_011529437.1:c.1567_1568del	XP_011527739.1:p.Leu523ThrfsTer?
XM_011529438.1:c.1438_1439del	XP_011527740.1:p.Leu480ThrfsTer?
XM_011529439.1:c.1054_1055del	XP_011527741.1:p.Leu352ThrfsTer?
XR_937433.1:n.1750_1751del
NM_001320412.1:c.1318_1319del	NP_001307341.1:p.Leu440ThrfsTer?
XM_006723961.4:c.1567_1568del	XP_006724024.2:p.Leu523ThrfsTer?
XM_006723962.4:c.1567_1568del	XP_006724025.2:p.Leu523ThrfsTer?
XM_011529434.3:c.1567_1568del	XP_011527736.1:p.Leu523ThrfsTer?
XM_011529435.3:c.1438_1439del	XP_011527737.1:p.Leu480ThrfsTer?
XM_011529436.3:c.1567_1568del	XP_011527738.1:p.Leu523ThrfsTer?
XM_011529437.3:c.1567_1568del	XP_011527739.1:p.Leu523ThrfsTer?
XM_011529439.2:c.1054_1055del	XP_011527741.1:p.Leu352ThrfsTer?
XR_937433.3:n.1784_1785del
NM_206965.2:c.1318_1319del MANE Select	NP_996848.1:p.Leu440ThrfsTer?
NM_001320412.2:c.1318_1319del	NP_001307341.1:p.Leu440ThrfsTer?
NM_006657.3:c.1318_1319del	NP_006648.1:p.Leu440ThrfsTer?