Canonical Allele Identifier: CA2838875191

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138636_46138637del , CM000683.2:g.46138636_46138637del	GRCh38
NC_000021.8:g.47558550_47558551del , CM000683.1:g.47558550_47558551del	GRCh37
NC_000021.7:g.46382978_46382979del	NCBI36
NG_016191.1:g.21931_21932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-151_-150del	ENSP00000507070.1:n.-151_-150del
ENST00000494498.2:c.48_49del	ENSP00000507847.1:p.Ala17ProfsTer?
ENST00000397746.8:c.1314_1315del MANE Select	ENSP00000380854.3:p.Ala439ProfsTer?
ENST00000291670.9:c.1314_1315del	ENSP00000291670.5:p.Ala439ProfsTer?
ENST00000397743.1:c.1270_1271del	ENSP00000380851.1:p.Gly424ProfsTer6
ENST00000397746.7:c.1314_1315del	ENSP00000380854.3:p.Ala439ProfsTer?
ENST00000397748.5:c.1314_1315del	ENSP00000380856.1:p.Ala439ProfsTer?
ENST00000460011.5:n.643_644del
ENST00000488577.1:n.340_341del
ENST00000494498.1:n.615_616del
ENST00000498355.6:n.1383_1384del
NM_006657.2:c.1314_1315del	NP_006648.1:p.Ala439ProfsTer?
NM_206965.1:c.1314_1315del	NP_996848.1:p.Ala439ProfsTer?
XM_006723961.2:c.1563_1564del	XP_006724024.2:p.Ala522ProfsTer?
XM_006723962.2:c.1563_1564del	XP_006724025.2:p.Ala522ProfsTer?
XM_011529434.1:c.1563_1564del	XP_011527736.1:p.Ala522ProfsTer?
XM_011529435.1:c.1434_1435del	XP_011527737.1:p.Ala479ProfsTer?
XM_011529436.1:c.1563_1564del	XP_011527738.1:p.Ala522ProfsTer?
XM_011529437.1:c.1563_1564del	XP_011527739.1:p.Ala522ProfsTer?
XM_011529438.1:c.1434_1435del	XP_011527740.1:p.Ala479ProfsTer?
XM_011529439.1:c.1050_1051del	XP_011527741.1:p.Ala351ProfsTer?
XR_937433.1:n.1746_1747del
NM_001320412.1:c.1314_1315del	NP_001307341.1:p.Ala439ProfsTer?
XM_006723961.4:c.1563_1564del	XP_006724024.2:p.Ala522ProfsTer?
XM_006723962.4:c.1563_1564del	XP_006724025.2:p.Ala522ProfsTer?
XM_011529434.3:c.1563_1564del	XP_011527736.1:p.Ala522ProfsTer?
XM_011529435.3:c.1434_1435del	XP_011527737.1:p.Ala479ProfsTer?
XM_011529436.3:c.1563_1564del	XP_011527738.1:p.Ala522ProfsTer?
XM_011529437.3:c.1563_1564del	XP_011527739.1:p.Ala522ProfsTer?
XM_011529439.2:c.1050_1051del	XP_011527741.1:p.Ala351ProfsTer?
XR_937433.3:n.1780_1781del
NM_206965.2:c.1314_1315del MANE Select	NP_996848.1:p.Ala439ProfsTer?
NM_001320412.2:c.1314_1315del	NP_001307341.1:p.Ala439ProfsTer?
NM_006657.3:c.1314_1315del	NP_006648.1:p.Ala439ProfsTer?