Canonical Allele Identifier: CA2392518384

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138427_46138428delinsAC , CM000683.2:g.46138427_46138428delinsAC	GRCh38
NC_000021.8:g.47558341_47558342delinsAC , CM000683.1:g.47558341_47558342delinsAC	GRCh37
NC_000021.7:g.46382769_46382770delinsAC	NCBI36
NG_016191.1:g.22140_22141delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-22+80_-22+81delinsGT	ENSP00000507070.1:n.-22+80_-22+81delinsGT
ENST00000494498.2:c.177+80_177+81delinsGT	ENSP00000507847.1:n.177+80_177+81delinsGT
ENST00000397746.8:c.1443+80_1443+81delinsGT MANE Select	ENSP00000380854.3:n.1443+80_1443+81delinsGT
ENST00000291670.9:c.1443+80_1443+81delinsGT	ENSP00000291670.5:n.1443+80_1443+81delinsGT
ENST00000397743.1:c.1399+80_1399+81delinsGT	ENSP00000380851.1:n.1399+80_1399+81delinsGT
ENST00000397746.7:c.1443+80_1443+81delinsGT	ENSP00000380854.3:n.1443+80_1443+81delinsGT
ENST00000397748.5:c.1443+80_1443+81delinsGT	ENSP00000380856.1:n.1443+80_1443+81delinsGT
ENST00000446405.5:c.65+80_65+81delinsGT
ENST00000460011.5:n.772+80_772+81delinsGT
ENST00000494498.1:n.744+80_744+81delinsGT
ENST00000498355.6:n.1512+80_1512+81delinsGT
NM_006657.2:c.1443+80_1443+81delinsGT	NP_006648.1:n.1443+80_1443+81delinsGT
NM_206965.1:c.1443+80_1443+81delinsGT	NP_996848.1:n.1443+80_1443+81delinsGT
XM_006723961.2:c.1692+80_1692+81delinsGT	XP_006724024.2:n.1692+80_1692+81delinsGT
XM_006723962.2:c.1692+80_1692+81delinsGT	XP_006724025.2:n.1692+80_1692+81delinsGT
XM_011529434.1:c.1692+80_1692+81delinsGT	XP_011527736.1:n.1692+80_1692+81delinsGT
XM_011529435.1:c.1563+80_1563+81delinsGT	XP_011527737.1:n.1563+80_1563+81delinsGT
XM_011529436.1:c.1692+80_1692+81delinsGT	XP_011527738.1:n.1692+80_1692+81delinsGT
XM_011529437.1:c.1692+80_1692+81delinsGT	XP_011527739.1:n.1692+80_1692+81delinsGT
XM_011529438.1:c.1563+80_1563+81delinsGT	XP_011527740.1:n.1563+80_1563+81delinsGT
XM_011529439.1:c.1179+80_1179+81delinsGT	XP_011527741.1:n.1179+80_1179+81delinsGT
XR_937433.1:n.1875+80_1875+81delinsGT
NM_001320412.1:c.1443+80_1443+81delinsGT	NP_001307341.1:n.1443+80_1443+81delinsGT
XM_006723961.4:c.1692+80_1692+81delinsGT	XP_006724024.2:n.1692+80_1692+81delinsGT
XM_006723962.4:c.1692+80_1692+81delinsGT	XP_006724025.2:n.1692+80_1692+81delinsGT
XM_011529434.3:c.1692+80_1692+81delinsGT	XP_011527736.1:n.1692+80_1692+81delinsGT
XM_011529435.3:c.1563+80_1563+81delinsGT	XP_011527737.1:n.1563+80_1563+81delinsGT
XM_011529436.3:c.1692+80_1692+81delinsGT	XP_011527738.1:n.1692+80_1692+81delinsGT
XM_011529437.3:c.1692+80_1692+81delinsGT	XP_011527739.1:n.1692+80_1692+81delinsGT
XM_011529439.2:c.1179+80_1179+81delinsGT	XP_011527741.1:n.1179+80_1179+81delinsGT
XR_937433.3:n.1909+80_1909+81delinsGT
NM_206965.2:c.1443+80_1443+81delinsGT MANE Select	NP_996848.1:n.1443+80_1443+81delinsGT
NM_001320412.2:c.1443+80_1443+81delinsGT	NP_001307341.1:n.1443+80_1443+81delinsGT
NM_006657.3:c.1443+80_1443+81delinsGT	NP_006648.1:n.1443+80_1443+81delinsGT