Canonical Allele Identifier: CA2654977185

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138680-G-GGCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138681_46138684dup , CM000683.2:g.46138681_46138684dup	GRCh38
NC_000021.8:g.47558595_47558598dup , CM000683.1:g.47558595_47558598dup	GRCh37
NC_000021.7:g.46383023_46383026dup	NCBI36
NG_016191.1:g.21884_21887dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-38_-160-35dup	ENSP00000507070.1:n.-160-38_-160-35dup
ENST00000494498.2:c.39-38_39-35dup	ENSP00000507847.1:n.39-38_39-35dup
ENST00000397746.8:c.1305-38_1305-35dup MANE Select	ENSP00000380854.3:n.1305-38_1305-35dup
ENST00000291670.9:c.1305-38_1305-35dup	ENSP00000291670.5:n.1305-38_1305-35dup
ENST00000397743.1:c.1261-38_1261-35dup	ENSP00000380851.1:n.1261-38_1261-35dup
ENST00000397746.7:c.1305-38_1305-35dup	ENSP00000380854.3:n.1305-38_1305-35dup
ENST00000397748.5:c.1305-38_1305-35dup	ENSP00000380856.1:n.1305-38_1305-35dup
ENST00000460011.5:n.634-38_634-35dup
ENST00000488577.1:n.331-38_331-35dup
ENST00000494498.1:n.606-38_606-35dup
ENST00000498355.6:n.1374-38_1374-35dup
NM_006657.2:c.1305-38_1305-35dup	NP_006648.1:n.1305-38_1305-35dup
NM_206965.1:c.1305-38_1305-35dup	NP_996848.1:n.1305-38_1305-35dup
XM_006723961.2:c.1554-38_1554-35dup	XP_006724024.2:n.1554-38_1554-35dup
XM_006723962.2:c.1554-38_1554-35dup	XP_006724025.2:n.1554-38_1554-35dup
XM_011529434.1:c.1554-38_1554-35dup	XP_011527736.1:n.1554-38_1554-35dup
XM_011529435.1:c.1425-38_1425-35dup	XP_011527737.1:n.1425-38_1425-35dup
XM_011529436.1:c.1554-38_1554-35dup	XP_011527738.1:n.1554-38_1554-35dup
XM_011529437.1:c.1554-38_1554-35dup	XP_011527739.1:n.1554-38_1554-35dup
XM_011529438.1:c.1425-38_1425-35dup	XP_011527740.1:n.1425-38_1425-35dup
XM_011529439.1:c.1041-38_1041-35dup	XP_011527741.1:n.1041-38_1041-35dup
XR_937433.1:n.1737-38_1737-35dup
NM_001320412.1:c.1305-38_1305-35dup	NP_001307341.1:n.1305-38_1305-35dup
XM_006723961.4:c.1554-38_1554-35dup	XP_006724024.2:n.1554-38_1554-35dup
XM_006723962.4:c.1554-38_1554-35dup	XP_006724025.2:n.1554-38_1554-35dup
XM_011529434.3:c.1554-38_1554-35dup	XP_011527736.1:n.1554-38_1554-35dup
XM_011529435.3:c.1425-38_1425-35dup	XP_011527737.1:n.1425-38_1425-35dup
XM_011529436.3:c.1554-38_1554-35dup	XP_011527738.1:n.1554-38_1554-35dup
XM_011529437.3:c.1554-38_1554-35dup	XP_011527739.1:n.1554-38_1554-35dup
XM_011529439.2:c.1041-38_1041-35dup	XP_011527741.1:n.1041-38_1041-35dup
XR_937433.3:n.1771-38_1771-35dup
NM_206965.2:c.1305-38_1305-35dup MANE Select	NP_996848.1:n.1305-38_1305-35dup
NM_001320412.2:c.1305-38_1305-35dup	NP_001307341.1:n.1305-38_1305-35dup
NM_006657.3:c.1305-38_1305-35dup	NP_006648.1:n.1305-38_1305-35dup