Canonical Allele Identifier: CA2392518181

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138137_46138143delinsCGCCTCA , CM000683.2:g.46138137_46138143delinsCGCCTCA	GRCh38
NC_000021.8:g.47558051_47558057delinsCGCCTCA , CM000683.1:g.47558051_47558057delinsCGCCTCA	GRCh37
NC_000021.7:g.46382479_46382485delinsCGCCTCA	NCBI36
NG_016191.1:g.22425_22431delinsTGAGGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-22+365_-22+371delinsTGAGGCG	ENSP00000507070.1:n.-22+365_-22+371delinsTGAGGCG
ENST00000494498.2:c.177+365_177+371delinsTGAGGCG	ENSP00000507847.1:n.177+365_177+371delinsTGAGGCG
ENST00000397746.8:c.1443+365_1443+371delinsTGAGGCG MANE Select	ENSP00000380854.3:n.1443+365_1443+371delinsTGAGGCG
ENST00000291670.9:c.1443+365_1443+371delinsTGAGGCG	ENSP00000291670.5:n.1443+365_1443+371delinsTGAGGCG
ENST00000397743.1:c.1399+365_1399+371delinsTGAGGCG	ENSP00000380851.1:n.1399+365_1399+371delinsTGAGGCG
ENST00000397746.7:c.1443+365_1443+371delinsTGAGGCG	ENSP00000380854.3:n.1443+365_1443+371delinsTGAGGCG
ENST00000397748.5:c.1443+365_1443+371delinsTGAGGCG	ENSP00000380856.1:n.1443+365_1443+371delinsTGAGGCG
ENST00000446405.5:c.65+365_65+371delinsTGAGGCG
ENST00000460011.5:n.772+365_772+371delinsTGAGGCG
ENST00000494498.1:n.744+365_744+371delinsTGAGGCG
ENST00000498355.6:n.1512+365_1512+371delinsTGAGGCG
NM_006657.2:c.1443+365_1443+371delinsTGAGGCG	NP_006648.1:n.1443+365_1443+371delinsTGAGGCG
NM_206965.1:c.1443+365_1443+371delinsTGAGGCG	NP_996848.1:n.1443+365_1443+371delinsTGAGGCG
XM_006723961.2:c.1692+365_1692+371delinsTGAGGCG	XP_006724024.2:n.1692+365_1692+371delinsTGAGGCG
XM_006723962.2:c.1692+365_1692+371delinsTGAGGCG	XP_006724025.2:n.1692+365_1692+371delinsTGAGGCG
XM_011529434.1:c.1692+365_1692+371delinsTGAGGCG	XP_011527736.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529435.1:c.1563+365_1563+371delinsTGAGGCG	XP_011527737.1:n.1563+365_1563+371delinsTGAGGCG
XM_011529436.1:c.1692+365_1692+371delinsTGAGGCG	XP_011527738.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529437.1:c.1692+365_1692+371delinsTGAGGCG	XP_011527739.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529438.1:c.1563+365_1563+371delinsTGAGGCG	XP_011527740.1:n.1563+365_1563+371delinsTGAGGCG
XM_011529439.1:c.1179+365_1179+371delinsTGAGGCG	XP_011527741.1:n.1179+365_1179+371delinsTGAGGCG
XR_937433.1:n.1875+365_1875+371delinsTGAGGCG
NM_001320412.1:c.1443+365_1443+371delinsTGAGGCG	NP_001307341.1:n.1443+365_1443+371delinsTGAGGCG
XM_006723961.4:c.1692+365_1692+371delinsTGAGGCG	XP_006724024.2:n.1692+365_1692+371delinsTGAGGCG
XM_006723962.4:c.1692+365_1692+371delinsTGAGGCG	XP_006724025.2:n.1692+365_1692+371delinsTGAGGCG
XM_011529434.3:c.1692+365_1692+371delinsTGAGGCG	XP_011527736.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529435.3:c.1563+365_1563+371delinsTGAGGCG	XP_011527737.1:n.1563+365_1563+371delinsTGAGGCG
XM_011529436.3:c.1692+365_1692+371delinsTGAGGCG	XP_011527738.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529437.3:c.1692+365_1692+371delinsTGAGGCG	XP_011527739.1:n.1692+365_1692+371delinsTGAGGCG
XM_011529439.2:c.1179+365_1179+371delinsTGAGGCG	XP_011527741.1:n.1179+365_1179+371delinsTGAGGCG
XR_937433.3:n.1909+365_1909+371delinsTGAGGCG
NM_206965.2:c.1443+365_1443+371delinsTGAGGCG MANE Select	NP_996848.1:n.1443+365_1443+371delinsTGAGGCG
NM_001320412.2:c.1443+365_1443+371delinsTGAGGCG	NP_001307341.1:n.1443+365_1443+371delinsTGAGGCG
NM_006657.3:c.1443+365_1443+371delinsTGAGGCG	NP_006648.1:n.1443+365_1443+371delinsTGAGGCG