Canonical Allele Identifier: CA200957
Gene: FTCD HGNC NCBI

Linked Data

ClinVar Variation Id: 194078
dbSNP Id: rs777099958

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46138586dup , CM000683.2:g.46138586dup GRCh38
NC_000021.8:g.47558500dup , CM000683.1:g.47558500dup GRCh37
NC_000021.7:g.46382928dup NCBI36
NG_016191.1:g.21983dup

Transcript Alleles

HGVS Amino-acid change
ENST00000460011.6:c.-99dup ENSP00000507070.1:n.-99dup
ENST00000494498.2:c.100dup ENSP00000507847.1:p.Glu34GlyfsTer?
ENST00000397746.8:c.1366dup MANE Select ENSP00000380854.3:p.Glu456GlyfsTer?
ENST00000291670.9:c.1366dup ENSP00000291670.5:p.Glu456GlyfsTer?
ENST00000397743.1:c.1322dup ENSP00000380851.1:p.Asp442ArgfsTer?
ENST00000397746.7:c.1366dup ENSP00000380854.3:p.Glu456GlyfsTer?
ENST00000397748.5:c.1366dup ENSP00000380856.1:p.Glu456GlyfsTer?
ENST00000460011.5:n.695dup
ENST00000488577.1:n.392dup
ENST00000494498.1:n.667dup
ENST00000498355.6:n.1435dup
NM_006657.2:c.1366dup NP_006648.1:p.Glu456GlyfsTer?
NM_206965.1:c.1366dup NP_996848.1:p.Glu456GlyfsTer?
XM_006723961.2:c.1615dup XP_006724024.2:p.Glu539GlyfsTer?
XM_006723962.2:c.1615dup XP_006724025.2:p.Glu539GlyfsTer?
XM_011529434.1:c.1615dup XP_011527736.1:p.Glu539GlyfsTer?
XM_011529435.1:c.1486dup XP_011527737.1:p.Glu496GlyfsTer?
XM_011529436.1:c.1615dup XP_011527738.1:p.Glu539GlyfsTer?
XM_011529437.1:c.1615dup XP_011527739.1:p.Glu539GlyfsTer?
XM_011529438.1:c.1486dup XP_011527740.1:p.Glu496GlyfsTer?
XM_011529439.1:c.1102dup XP_011527741.1:p.Glu368GlyfsTer?
XR_937433.1:n.1798dup
NM_001320412.1:c.1366dup NP_001307341.1:p.Glu456GlyfsTer?
XM_006723961.4:c.1615dup XP_006724024.2:p.Glu539GlyfsTer?
XM_006723962.4:c.1615dup XP_006724025.2:p.Glu539GlyfsTer?
XM_011529434.3:c.1615dup XP_011527736.1:p.Glu539GlyfsTer?
XM_011529435.3:c.1486dup XP_011527737.1:p.Glu496GlyfsTer?
XM_011529436.3:c.1615dup XP_011527738.1:p.Glu539GlyfsTer?
XM_011529437.3:c.1615dup XP_011527739.1:p.Glu539GlyfsTer?
XM_011529439.2:c.1102dup XP_011527741.1:p.Glu368GlyfsTer?
XR_937433.3:n.1832dup
NM_206965.2:c.1366dup MANE Select NP_996848.1:p.Glu456GlyfsTer?
NM_001320412.2:c.1366dup NP_001307341.1:p.Glu456GlyfsTer?
NM_006657.3:c.1366dup NP_006648.1:p.Glu456GlyfsTer?