Canonical Allele Identifier: CA2818102617

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138645del , CM000683.2:g.46138645del	GRCh38
NC_000021.8:g.47558559del , CM000683.1:g.47558559del	GRCh37
NC_000021.7:g.46382987del	NCBI36
NG_016191.1:g.21923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-159del	ENSP00000507070.1:n.-159del
ENST00000494498.2:c.40del	ENSP00000507847.1:p.Arg14AlafsTer9
ENST00000397746.8:c.1306del MANE Select	ENSP00000380854.3:p.Arg436AlafsTer9
ENST00000291670.9:c.1306del	ENSP00000291670.5:p.Arg436AlafsTer9
ENST00000397743.1:c.1262del	ENSP00000380851.1:p.Ala421GlyfsTer?
ENST00000397746.7:c.1306del	ENSP00000380854.3:p.Arg436AlafsTer9
ENST00000397748.5:c.1306del	ENSP00000380856.1:p.Arg436AlafsTer9
ENST00000460011.5:n.635del
ENST00000488577.1:n.332del
ENST00000494498.1:n.607del
ENST00000498355.6:n.1375del
NM_006657.2:c.1306del	NP_006648.1:p.Arg436AlafsTer9
NM_206965.1:c.1306del	NP_996848.1:p.Arg436AlafsTer9
XM_006723961.2:c.1555del	XP_006724024.2:p.Arg519AlafsTer9
XM_006723962.2:c.1555del	XP_006724025.2:p.Arg519AlafsTer9
XM_011529434.1:c.1555del	XP_011527736.1:p.Arg519AlafsTer9
XM_011529435.1:c.1426del	XP_011527737.1:p.Arg476AlafsTer9
XM_011529436.1:c.1555del	XP_011527738.1:p.Arg519AlafsTer9
XM_011529437.1:c.1555del	XP_011527739.1:p.Arg519AlafsTer9
XM_011529438.1:c.1426del	XP_011527740.1:p.Arg476AlafsTer9
XM_011529439.1:c.1042del	XP_011527741.1:p.Arg348AlafsTer9
XR_937433.1:n.1738del
NM_001320412.1:c.1306del	NP_001307341.1:p.Arg436AlafsTer9
XM_006723961.4:c.1555del	XP_006724024.2:p.Arg519AlafsTer9
XM_006723962.4:c.1555del	XP_006724025.2:p.Arg519AlafsTer9
XM_011529434.3:c.1555del	XP_011527736.1:p.Arg519AlafsTer9
XM_011529435.3:c.1426del	XP_011527737.1:p.Arg476AlafsTer9
XM_011529436.3:c.1555del	XP_011527738.1:p.Arg519AlafsTer9
XM_011529437.3:c.1555del	XP_011527739.1:p.Arg519AlafsTer9
XM_011529439.2:c.1042del	XP_011527741.1:p.Arg348AlafsTer9
XR_937433.3:n.1772del
NM_206965.2:c.1306del MANE Select	NP_996848.1:p.Arg436AlafsTer9
NM_001320412.2:c.1306del	NP_001307341.1:p.Arg436AlafsTer9
NM_006657.3:c.1306del	NP_006648.1:p.Arg436AlafsTer9