Canonical Allele Identifier: CA2654976858

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138429-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138429_46138430insAG , CM000683.2:g.46138429_46138430insAG	GRCh38
NC_000021.8:g.47558343_47558344insAG , CM000683.1:g.47558343_47558344insAG	GRCh37
NC_000021.7:g.46382771_46382772insAG	NCBI36
NG_016191.1:g.22138_22139insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-22+78_-22+79insCT	ENSP00000507070.1:n.-22+78_-22+79insCT
ENST00000494498.2:c.177+78_177+79insCT	ENSP00000507847.1:n.177+78_177+79insCT
ENST00000397746.8:c.1443+78_1443+79insCT MANE Select	ENSP00000380854.3:n.1443+78_1443+79insCT
ENST00000291670.9:c.1443+78_1443+79insCT	ENSP00000291670.5:n.1443+78_1443+79insCT
ENST00000397743.1:c.1399+78_1399+79insCT	ENSP00000380851.1:n.1399+78_1399+79insCT
ENST00000397746.7:c.1443+78_1443+79insCT	ENSP00000380854.3:n.1443+78_1443+79insCT
ENST00000397748.5:c.1443+78_1443+79insCT	ENSP00000380856.1:n.1443+78_1443+79insCT
ENST00000446405.5:c.65+78_65+79insCT
ENST00000460011.5:n.772+78_772+79insCT
ENST00000494498.1:n.744+78_744+79insCT
ENST00000498355.6:n.1512+78_1512+79insCT
NM_006657.2:c.1443+78_1443+79insCT	NP_006648.1:n.1443+78_1443+79insCT
NM_206965.1:c.1443+78_1443+79insCT	NP_996848.1:n.1443+78_1443+79insCT
XM_006723961.2:c.1692+78_1692+79insCT	XP_006724024.2:n.1692+78_1692+79insCT
XM_006723962.2:c.1692+78_1692+79insCT	XP_006724025.2:n.1692+78_1692+79insCT
XM_011529434.1:c.1692+78_1692+79insCT	XP_011527736.1:n.1692+78_1692+79insCT
XM_011529435.1:c.1563+78_1563+79insCT	XP_011527737.1:n.1563+78_1563+79insCT
XM_011529436.1:c.1692+78_1692+79insCT	XP_011527738.1:n.1692+78_1692+79insCT
XM_011529437.1:c.1692+78_1692+79insCT	XP_011527739.1:n.1692+78_1692+79insCT
XM_011529438.1:c.1563+78_1563+79insCT	XP_011527740.1:n.1563+78_1563+79insCT
XM_011529439.1:c.1179+78_1179+79insCT	XP_011527741.1:n.1179+78_1179+79insCT
XR_937433.1:n.1875+78_1875+79insCT
NM_001320412.1:c.1443+78_1443+79insCT	NP_001307341.1:n.1443+78_1443+79insCT
XM_006723961.4:c.1692+78_1692+79insCT	XP_006724024.2:n.1692+78_1692+79insCT
XM_006723962.4:c.1692+78_1692+79insCT	XP_006724025.2:n.1692+78_1692+79insCT
XM_011529434.3:c.1692+78_1692+79insCT	XP_011527736.1:n.1692+78_1692+79insCT
XM_011529435.3:c.1563+78_1563+79insCT	XP_011527737.1:n.1563+78_1563+79insCT
XM_011529436.3:c.1692+78_1692+79insCT	XP_011527738.1:n.1692+78_1692+79insCT
XM_011529437.3:c.1692+78_1692+79insCT	XP_011527739.1:n.1692+78_1692+79insCT
XM_011529439.2:c.1179+78_1179+79insCT	XP_011527741.1:n.1179+78_1179+79insCT
XR_937433.3:n.1909+78_1909+79insCT
NM_206965.2:c.1443+78_1443+79insCT MANE Select	NP_996848.1:n.1443+78_1443+79insCT
NM_001320412.2:c.1443+78_1443+79insCT	NP_001307341.1:n.1443+78_1443+79insCT
NM_006657.3:c.1443+78_1443+79insCT	NP_006648.1:n.1443+78_1443+79insCT