Canonical Allele Identifier: CA2654976814

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138393-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138395_46138396del , CM000683.2:g.46138395_46138396del	GRCh38
NC_000021.8:g.47558309_47558310del , CM000683.1:g.47558309_47558310del	GRCh37
NC_000021.7:g.46382737_46382738del	NCBI36
NG_016191.1:g.22173_22174del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-22+113_-22+114del	ENSP00000507070.1:n.-22+113_-22+114del
ENST00000494498.2:c.177+113_177+114del	ENSP00000507847.1:n.177+113_177+114del
ENST00000397746.8:c.1443+113_1443+114del MANE Select	ENSP00000380854.3:n.1443+113_1443+114del
ENST00000291670.9:c.1443+113_1443+114del	ENSP00000291670.5:n.1443+113_1443+114del
ENST00000397743.1:c.1399+113_1399+114del	ENSP00000380851.1:n.1399+113_1399+114del
ENST00000397746.7:c.1443+113_1443+114del	ENSP00000380854.3:n.1443+113_1443+114del
ENST00000397748.5:c.1443+113_1443+114del	ENSP00000380856.1:n.1443+113_1443+114del
ENST00000446405.5:c.65+113_65+114del
ENST00000460011.5:n.772+113_772+114del
ENST00000494498.1:n.744+113_744+114del
ENST00000498355.6:n.1512+113_1512+114del
NM_006657.2:c.1443+113_1443+114del	NP_006648.1:n.1443+113_1443+114del
NM_206965.1:c.1443+113_1443+114del	NP_996848.1:n.1443+113_1443+114del
XM_006723961.2:c.1692+113_1692+114del	XP_006724024.2:n.1692+113_1692+114del
XM_006723962.2:c.1692+113_1692+114del	XP_006724025.2:n.1692+113_1692+114del
XM_011529434.1:c.1692+113_1692+114del	XP_011527736.1:n.1692+113_1692+114del
XM_011529435.1:c.1563+113_1563+114del	XP_011527737.1:n.1563+113_1563+114del
XM_011529436.1:c.1692+113_1692+114del	XP_011527738.1:n.1692+113_1692+114del
XM_011529437.1:c.1692+113_1692+114del	XP_011527739.1:n.1692+113_1692+114del
XM_011529438.1:c.1563+113_1563+114del	XP_011527740.1:n.1563+113_1563+114del
XM_011529439.1:c.1179+113_1179+114del	XP_011527741.1:n.1179+113_1179+114del
XR_937433.1:n.1875+113_1875+114del
NM_001320412.1:c.1443+113_1443+114del	NP_001307341.1:n.1443+113_1443+114del
XM_006723961.4:c.1692+113_1692+114del	XP_006724024.2:n.1692+113_1692+114del
XM_006723962.4:c.1692+113_1692+114del	XP_006724025.2:n.1692+113_1692+114del
XM_011529434.3:c.1692+113_1692+114del	XP_011527736.1:n.1692+113_1692+114del
XM_011529435.3:c.1563+113_1563+114del	XP_011527737.1:n.1563+113_1563+114del
XM_011529436.3:c.1692+113_1692+114del	XP_011527738.1:n.1692+113_1692+114del
XM_011529437.3:c.1692+113_1692+114del	XP_011527739.1:n.1692+113_1692+114del
XM_011529439.2:c.1179+113_1179+114del	XP_011527741.1:n.1179+113_1179+114del
XR_937433.3:n.1909+113_1909+114del
NM_206965.2:c.1443+113_1443+114del MANE Select	NP_996848.1:n.1443+113_1443+114del
NM_001320412.2:c.1443+113_1443+114del	NP_001307341.1:n.1443+113_1443+114del
NM_006657.3:c.1443+113_1443+114del	NP_006648.1:n.1443+113_1443+114del