Canonical Allele Identifier: CA2392518545

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138658_46138663delinsAAGAGG , CM000683.2:g.46138658_46138663delinsAAGAGG	GRCh38
NC_000021.8:g.47558572_47558577delinsAAGAGG , CM000683.1:g.47558572_47558577delinsAAGAGG	GRCh37
NC_000021.7:g.46383000_46383005delinsAAGAGG	NCBI36
NG_016191.1:g.21905_21910delinsCCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-17_-160-12delinsCCTCTT	ENSP00000507070.1:n.-160-17_-160-12delinsCCTCTT
ENST00000494498.2:c.39-17_39-12delinsCCTCTT	ENSP00000507847.1:n.39-17_39-12delinsCCTCTT
ENST00000397746.8:c.1305-17_1305-12delinsCCTCTT MANE Select	ENSP00000380854.3:n.1305-17_1305-12delinsCCTCTT
ENST00000291670.9:c.1305-17_1305-12delinsCCTCTT	ENSP00000291670.5:n.1305-17_1305-12delinsCCTCTT
ENST00000397743.1:c.1261-17_1261-12delinsCCTCTT	ENSP00000380851.1:n.1261-17_1261-12delinsCCTCTT
ENST00000397746.7:c.1305-17_1305-12delinsCCTCTT	ENSP00000380854.3:n.1305-17_1305-12delinsCCTCTT
ENST00000397748.5:c.1305-17_1305-12delinsCCTCTT	ENSP00000380856.1:n.1305-17_1305-12delinsCCTCTT
ENST00000460011.5:n.634-17_634-12delinsCCTCTT
ENST00000488577.1:n.331-17_331-12delinsCCTCTT
ENST00000494498.1:n.606-17_606-12delinsCCTCTT
ENST00000498355.6:n.1374-17_1374-12delinsCCTCTT
NM_006657.2:c.1305-17_1305-12delinsCCTCTT	NP_006648.1:n.1305-17_1305-12delinsCCTCTT
NM_206965.1:c.1305-17_1305-12delinsCCTCTT	NP_996848.1:n.1305-17_1305-12delinsCCTCTT
XM_006723961.2:c.1554-17_1554-12delinsCCTCTT	XP_006724024.2:n.1554-17_1554-12delinsCCTCTT
XM_006723962.2:c.1554-17_1554-12delinsCCTCTT	XP_006724025.2:n.1554-17_1554-12delinsCCTCTT
XM_011529434.1:c.1554-17_1554-12delinsCCTCTT	XP_011527736.1:n.1554-17_1554-12delinsCCTCTT
XM_011529435.1:c.1425-17_1425-12delinsCCTCTT	XP_011527737.1:n.1425-17_1425-12delinsCCTCTT
XM_011529436.1:c.1554-17_1554-12delinsCCTCTT	XP_011527738.1:n.1554-17_1554-12delinsCCTCTT
XM_011529437.1:c.1554-17_1554-12delinsCCTCTT	XP_011527739.1:n.1554-17_1554-12delinsCCTCTT
XM_011529438.1:c.1425-17_1425-12delinsCCTCTT	XP_011527740.1:n.1425-17_1425-12delinsCCTCTT
XM_011529439.1:c.1041-17_1041-12delinsCCTCTT	XP_011527741.1:n.1041-17_1041-12delinsCCTCTT
XR_937433.1:n.1737-17_1737-12delinsCCTCTT
NM_001320412.1:c.1305-17_1305-12delinsCCTCTT	NP_001307341.1:n.1305-17_1305-12delinsCCTCTT
XM_006723961.4:c.1554-17_1554-12delinsCCTCTT	XP_006724024.2:n.1554-17_1554-12delinsCCTCTT
XM_006723962.4:c.1554-17_1554-12delinsCCTCTT	XP_006724025.2:n.1554-17_1554-12delinsCCTCTT
XM_011529434.3:c.1554-17_1554-12delinsCCTCTT	XP_011527736.1:n.1554-17_1554-12delinsCCTCTT
XM_011529435.3:c.1425-17_1425-12delinsCCTCTT	XP_011527737.1:n.1425-17_1425-12delinsCCTCTT
XM_011529436.3:c.1554-17_1554-12delinsCCTCTT	XP_011527738.1:n.1554-17_1554-12delinsCCTCTT
XM_011529437.3:c.1554-17_1554-12delinsCCTCTT	XP_011527739.1:n.1554-17_1554-12delinsCCTCTT
XM_011529439.2:c.1041-17_1041-12delinsCCTCTT	XP_011527741.1:n.1041-17_1041-12delinsCCTCTT
XR_937433.3:n.1771-17_1771-12delinsCCTCTT
NM_206965.2:c.1305-17_1305-12delinsCCTCTT MANE Select	NP_996848.1:n.1305-17_1305-12delinsCCTCTT
NM_001320412.2:c.1305-17_1305-12delinsCCTCTT	NP_001307341.1:n.1305-17_1305-12delinsCCTCTT
NM_006657.3:c.1305-17_1305-12delinsCCTCTT	NP_006648.1:n.1305-17_1305-12delinsCCTCTT