Canonical Allele Identifier: CA2818102619

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138655_46138668del , CM000683.2:g.46138655_46138668del	GRCh38
NC_000021.8:g.47558569_47558582del , CM000683.1:g.47558569_47558582del	GRCh37
NC_000021.7:g.46382997_46383010del	NCBI36
NG_016191.1:g.21900_21913del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-22_-160-9del	ENSP00000507070.1:n.-160-22_-160-9del
ENST00000494498.2:c.39-22_39-9del	ENSP00000507847.1:n.39-22_39-9del
ENST00000397746.8:c.1305-22_1305-9del MANE Select	ENSP00000380854.3:n.1305-22_1305-9del
ENST00000291670.9:c.1305-22_1305-9del	ENSP00000291670.5:n.1305-22_1305-9del
ENST00000397743.1:c.1261-22_1261-9del	ENSP00000380851.1:n.1261-22_1261-9del
ENST00000397746.7:c.1305-22_1305-9del	ENSP00000380854.3:n.1305-22_1305-9del
ENST00000397748.5:c.1305-22_1305-9del	ENSP00000380856.1:n.1305-22_1305-9del
ENST00000460011.5:n.634-22_634-9del
ENST00000488577.1:n.331-22_331-9del
ENST00000494498.1:n.606-22_606-9del
ENST00000498355.6:n.1374-22_1374-9del
NM_006657.2:c.1305-22_1305-9del	NP_006648.1:n.1305-22_1305-9del
NM_206965.1:c.1305-22_1305-9del	NP_996848.1:n.1305-22_1305-9del
XM_006723961.2:c.1554-22_1554-9del	XP_006724024.2:n.1554-22_1554-9del
XM_006723962.2:c.1554-22_1554-9del	XP_006724025.2:n.1554-22_1554-9del
XM_011529434.1:c.1554-22_1554-9del	XP_011527736.1:n.1554-22_1554-9del
XM_011529435.1:c.1425-22_1425-9del	XP_011527737.1:n.1425-22_1425-9del
XM_011529436.1:c.1554-22_1554-9del	XP_011527738.1:n.1554-22_1554-9del
XM_011529437.1:c.1554-22_1554-9del	XP_011527739.1:n.1554-22_1554-9del
XM_011529438.1:c.1425-22_1425-9del	XP_011527740.1:n.1425-22_1425-9del
XM_011529439.1:c.1041-22_1041-9del	XP_011527741.1:n.1041-22_1041-9del
XR_937433.1:n.1737-22_1737-9del
NM_001320412.1:c.1305-22_1305-9del	NP_001307341.1:n.1305-22_1305-9del
XM_006723961.4:c.1554-22_1554-9del	XP_006724024.2:n.1554-22_1554-9del
XM_006723962.4:c.1554-22_1554-9del	XP_006724025.2:n.1554-22_1554-9del
XM_011529434.3:c.1554-22_1554-9del	XP_011527736.1:n.1554-22_1554-9del
XM_011529435.3:c.1425-22_1425-9del	XP_011527737.1:n.1425-22_1425-9del
XM_011529436.3:c.1554-22_1554-9del	XP_011527738.1:n.1554-22_1554-9del
XM_011529437.3:c.1554-22_1554-9del	XP_011527739.1:n.1554-22_1554-9del
XM_011529439.2:c.1041-22_1041-9del	XP_011527741.1:n.1041-22_1041-9del
XR_937433.3:n.1771-22_1771-9del
NM_206965.2:c.1305-22_1305-9del MANE Select	NP_996848.1:n.1305-22_1305-9del
NM_001320412.2:c.1305-22_1305-9del	NP_001307341.1:n.1305-22_1305-9del
NM_006657.3:c.1305-22_1305-9del	NP_006648.1:n.1305-22_1305-9del