Canonical Allele Identifier: CA410559022
Gene: FTCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46138584T>A , CM000683.2:g.46138584T>A GRCh38
NC_000021.8:g.47558498T>A , CM000683.1:g.47558498T>A GRCh37
NC_000021.7:g.46382926T>A NCBI36
NG_016191.1:g.21984A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000460011.6:c.-98A>T ENSP00000507070.1:n.-98A>T
ENST00000494498.2:c.101A>T ENSP00000507847.1:p.Glu34Val
ENST00000397746.8:c.1367A>T MANE Select ENSP00000380854.3:p.Glu456Val
ENST00000291670.9:c.1367A>T ENSP00000291670.5:p.Glu456Val
ENST00000397743.1:c.1323A>T ENSP00000380851.1:p.Gly441=
ENST00000397746.7:c.1367A>T ENSP00000380854.3:p.Glu456Val
ENST00000397748.5:c.1367A>T ENSP00000380856.1:p.Glu456Val
ENST00000460011.5:n.696A>T
ENST00000488577.1:n.393A>T
ENST00000494498.1:n.668A>T
ENST00000498355.6:n.1436A>T
NM_006657.2:c.1367A>T NP_006648.1:p.Glu456Val
NM_206965.1:c.1367A>T NP_996848.1:p.Glu456Val
XM_006723961.2:c.1616A>T XP_006724024.2:p.Glu539Val
XM_006723962.2:c.1616A>T XP_006724025.2:p.Glu539Val
XM_011529434.1:c.1616A>T XP_011527736.1:p.Glu539Val
XM_011529435.1:c.1487A>T XP_011527737.1:p.Glu496Val
XM_011529436.1:c.1616A>T XP_011527738.1:p.Glu539Val
XM_011529437.1:c.1616A>T XP_011527739.1:p.Glu539Val
XM_011529438.1:c.1487A>T XP_011527740.1:p.Glu496Val
XM_011529439.1:c.1103A>T XP_011527741.1:p.Glu368Val
XR_937433.1:n.1799A>T
NM_001320412.1:c.1367A>T NP_001307341.1:p.Glu456Val
XM_006723961.4:c.1616A>T XP_006724024.2:p.Glu539Val
XM_006723962.4:c.1616A>T XP_006724025.2:p.Glu539Val
XM_011529434.3:c.1616A>T XP_011527736.1:p.Glu539Val
XM_011529435.3:c.1487A>T XP_011527737.1:p.Glu496Val
XM_011529436.3:c.1616A>T XP_011527738.1:p.Glu539Val
XM_011529437.3:c.1616A>T XP_011527739.1:p.Glu539Val
XM_011529439.2:c.1103A>T XP_011527741.1:p.Glu368Val
XR_937433.3:n.1833A>T
NM_206965.2:c.1367A>T MANE Select NP_996848.1:p.Glu456Val
NM_001320412.2:c.1367A>T NP_001307341.1:p.Glu456Val
NM_006657.3:c.1367A>T NP_006648.1:p.Glu456Val