Canonical Allele Identifier: CA2654977271

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138757-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138757_46138758insC , CM000683.2:g.46138757_46138758insC	GRCh38
NC_000021.8:g.47558671_47558672insC , CM000683.1:g.47558671_47558672insC	GRCh37
NC_000021.7:g.46383099_46383100insC	NCBI36
NG_016191.1:g.21810_21811insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-112_-160-111insG	ENSP00000507070.1:n.-160-112_-160-111insG
ENST00000494498.2:c.39-112_39-111insG	ENSP00000507847.1:n.39-112_39-111insG
ENST00000397746.8:c.1305-112_1305-111insG MANE Select	ENSP00000380854.3:n.1305-112_1305-111insG
ENST00000291670.9:c.1305-112_1305-111insG	ENSP00000291670.5:n.1305-112_1305-111insG
ENST00000397743.1:c.1261-112_1261-111insG	ENSP00000380851.1:n.1261-112_1261-111insG
ENST00000397746.7:c.1305-112_1305-111insG	ENSP00000380854.3:n.1305-112_1305-111insG
ENST00000397748.5:c.1305-112_1305-111insG	ENSP00000380856.1:n.1305-112_1305-111insG
ENST00000460011.5:n.634-112_634-111insG
ENST00000488577.1:n.331-112_331-111insG
ENST00000494498.1:n.606-112_606-111insG
ENST00000498355.6:n.1374-112_1374-111insG
NM_006657.2:c.1305-112_1305-111insG	NP_006648.1:n.1305-112_1305-111insG
NM_206965.1:c.1305-112_1305-111insG	NP_996848.1:n.1305-112_1305-111insG
XM_006723961.2:c.1554-112_1554-111insG	XP_006724024.2:n.1554-112_1554-111insG
XM_006723962.2:c.1554-112_1554-111insG	XP_006724025.2:n.1554-112_1554-111insG
XM_011529434.1:c.1554-112_1554-111insG	XP_011527736.1:n.1554-112_1554-111insG
XM_011529435.1:c.1425-112_1425-111insG	XP_011527737.1:n.1425-112_1425-111insG
XM_011529436.1:c.1554-112_1554-111insG	XP_011527738.1:n.1554-112_1554-111insG
XM_011529437.1:c.1554-112_1554-111insG	XP_011527739.1:n.1554-112_1554-111insG
XM_011529438.1:c.1425-112_1425-111insG	XP_011527740.1:n.1425-112_1425-111insG
XM_011529439.1:c.1041-112_1041-111insG	XP_011527741.1:n.1041-112_1041-111insG
XR_937433.1:n.1737-112_1737-111insG
NM_001320412.1:c.1305-112_1305-111insG	NP_001307341.1:n.1305-112_1305-111insG
XM_006723961.4:c.1554-112_1554-111insG	XP_006724024.2:n.1554-112_1554-111insG
XM_006723962.4:c.1554-112_1554-111insG	XP_006724025.2:n.1554-112_1554-111insG
XM_011529434.3:c.1554-112_1554-111insG	XP_011527736.1:n.1554-112_1554-111insG
XM_011529435.3:c.1425-112_1425-111insG	XP_011527737.1:n.1425-112_1425-111insG
XM_011529436.3:c.1554-112_1554-111insG	XP_011527738.1:n.1554-112_1554-111insG
XM_011529437.3:c.1554-112_1554-111insG	XP_011527739.1:n.1554-112_1554-111insG
XM_011529439.2:c.1041-112_1041-111insG	XP_011527741.1:n.1041-112_1041-111insG
XR_937433.3:n.1771-112_1771-111insG
NM_206965.2:c.1305-112_1305-111insG MANE Select	NP_996848.1:n.1305-112_1305-111insG
NM_001320412.2:c.1305-112_1305-111insG	NP_001307341.1:n.1305-112_1305-111insG
NM_006657.3:c.1305-112_1305-111insG	NP_006648.1:n.1305-112_1305-111insG