Canonical Allele Identifier: CA2654985015

Gene: FTCD

Linked Data

• gnomAD v4: 21-46150292-G-GTAAAAAGTGAAATCTCATCTTCTGAACACA

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46150292_46150293insTAAAAAGTGAAATCTCATCTTCTGAACACA , CM000683.2:g.46150292_46150293insTAAAAAGTGAAATCTCATCTTCTGAACACA	GRCh38
NC_000021.8:g.47570206_47570207insTAAAAAGTGAAATCTCATCTTCTGAACACA , CM000683.1:g.47570206_47570207insTAAAAAGTGAAATCTCATCTTCTGAACACA	GRCh37
NC_000021.7:g.46394634_46394635insTAAAAAGTGAAATCTCATCTTCTGAACACA	NCBI36
NG_016191.1:g.10275_10276insTGTGTTCAGAAGATGAGATTTCACTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397746.8:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA MANE Select	ENSP00000380854.3:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACT...
ENST00000291670.9:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	ENSP00000291670.5:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACT...
ENST00000397743.1:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	ENSP00000380851.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACT...
ENST00000397746.7:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	ENSP00000380854.3:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACT...
ENST00000397748.5:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	ENSP00000380856.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACT...
ENST00000498355.6:n.844-43_844-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
NM_006657.2:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	NP_006648.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
NM_206965.1:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	NP_996848.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
XM_006723961.2:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_006724024.2:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_006723962.2:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_006724025.2:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529434.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527736.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529435.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527737.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529436.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527738.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529437.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527739.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529438.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527740.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529439.1:c.382-43_382-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527741.1:n.382-43_382-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529440.1:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527742.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XR_937433.1:n.1078-43_1078-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
NM_001320412.1:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	NP_001307341.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_006723961.4:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_006724024.2:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_006723962.4:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_006724025.2:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529434.3:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527736.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529435.3:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527737.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529436.3:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527738.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529437.3:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527739.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529439.2:c.382-43_382-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527741.1:n.382-43_382-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XM_011529440.3:c.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	XP_011527742.1:n.895-43_895-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
XR_937433.3:n.1112-43_1112-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
NM_206965.2:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA MANE Select	NP_996848.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA
NM_001320412.2:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	NP_001307341.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTT...
NM_006657.3:c.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA	NP_006648.1:n.775-43_775-42insTGTGTTCAGAAGATGAGATTTCACTTTTTA