Canonical Allele Identifier: CA2839872251

Gene: FTCD

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138644_46138645insCCAGGCTCTCCTCTTGCTCCTTTCAG , CM000683.2:g.46138644_46138645insCCAGGCTCTCCTCTTGCTCCTTTCAG	GRCh38
NC_000021.8:g.47558558_47558559insCCAGGCTCTCCTCTTGCTCCTTTCAG , CM000683.1:g.47558558_47558559insCCAGGCTCTCCTCTTGCTCCTTTCAG	GRCh37
NC_000021.7:g.46382986_46382987insCCAGGCTCTCCTCTTGCTCCTTTCAG	NCBI36
NG_016191.1:g.21923_21924insCTGAAAGGAGCAAGAGGAGAGCCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-159_-158insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000507070.1:n.-159_-158insCTGAAAGGAGCAAGAGGAGAGCCTGG
ENST00000494498.2:c.40_41insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000507847.1:p.Arg14ProfsTer18
ENST00000397746.8:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG MANE Select	ENSP00000380854.3:p.Arg436ProfsTer18
ENST00000291670.9:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000291670.5:p.Arg436ProfsTer18
ENST00000397743.1:c.1262_1263insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000380851.1:p.His422Ter
ENST00000397746.7:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000380854.3:p.Arg436ProfsTer18
ENST00000397748.5:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	ENSP00000380856.1:p.Arg436ProfsTer18
ENST00000460011.5:n.635_636insCTGAAAGGAGCAAGAGGAGAGCCTGG
ENST00000488577.1:n.332_333insCTGAAAGGAGCAAGAGGAGAGCCTGG
ENST00000494498.1:n.607_608insCTGAAAGGAGCAAGAGGAGAGCCTGG
ENST00000498355.6:n.1375_1376insCTGAAAGGAGCAAGAGGAGAGCCTGG
NM_006657.2:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	NP_006648.1:p.Arg436ProfsTer18
NM_206965.1:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	NP_996848.1:p.Arg436ProfsTer18
XM_006723961.2:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_006724024.2:p.Arg519ProfsTer18
XM_006723962.2:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_006724025.2:p.Arg519ProfsTer18
XM_011529434.1:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527736.1:p.Arg519ProfsTer18
XM_011529435.1:c.1426_1427insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527737.1:p.Arg476ProfsTer18
XM_011529436.1:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527738.1:p.Arg519ProfsTer18
XM_011529437.1:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527739.1:p.Arg519ProfsTer18
XM_011529438.1:c.1426_1427insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527740.1:p.Arg476ProfsTer18
XM_011529439.1:c.1042_1043insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527741.1:p.Arg348ProfsTer18
XR_937433.1:n.1738_1739insCTGAAAGGAGCAAGAGGAGAGCCTGG
NM_001320412.1:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	NP_001307341.1:p.Arg436ProfsTer18
XM_006723961.4:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_006724024.2:p.Arg519ProfsTer18
XM_006723962.4:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_006724025.2:p.Arg519ProfsTer18
XM_011529434.3:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527736.1:p.Arg519ProfsTer18
XM_011529435.3:c.1426_1427insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527737.1:p.Arg476ProfsTer18
XM_011529436.3:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527738.1:p.Arg519ProfsTer18
XM_011529437.3:c.1555_1556insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527739.1:p.Arg519ProfsTer18
XM_011529439.2:c.1042_1043insCTGAAAGGAGCAAGAGGAGAGCCTGG	XP_011527741.1:p.Arg348ProfsTer18
XR_937433.3:n.1772_1773insCTGAAAGGAGCAAGAGGAGAGCCTGG
NM_206965.2:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG MANE Select	NP_996848.1:p.Arg436ProfsTer18
NM_001320412.2:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	NP_001307341.1:p.Arg436ProfsTer18
NM_006657.3:c.1306_1307insCTGAAAGGAGCAAGAGGAGAGCCTGG	NP_006648.1:p.Arg436ProfsTer18