Canonical Allele Identifier: CA2392527127
Gene: FTCD HGNC NCBI
FTCD-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46151945G= , CM000683.2:g.46151945G= GRCh38
NC_000021.8:g.47571859G= , CM000683.1:g.47571859G= GRCh37
NC_000021.7:g.46396287G= NCBI36
NG_016191.1:g.8623C=

Transcript Alleles

HGVS Amino-acid Change
NM_206965.2:c.403C= (FTCD) MANE Select NP_996848.1:p.Arg135=
ENST00000397746.8:c.403C= (FTCD) MANE Select ENSP00000380854.3:p.Arg135=
NM_001320412.1:c.403C= (FTCD) NP_001307341.1:p.Arg135=
NM_001320412.2:c.403C= (FTCD) NP_001307341.1:p.Arg135=
NM_001350598.1:c.225+186G= (FTCD-AS1) NP_001337527.1:n.225+186G=
NM_006657.2:c.403C= (FTCD) NP_006648.1:p.Arg135=
NM_006657.3:c.403C= (FTCD) NP_006648.1:p.Arg135=
NM_206965.1:c.403C= (FTCD) NP_996848.1:p.Arg135=
NR_170989.1:n.146+186G= (FTCD-AS1)
ENST00000291670.9:c.403C= (FTCD) ENSP00000291670.5:p.Arg135=
ENST00000397743.1:c.403C= (FTCD) ENSP00000380851.1:p.Arg135=
ENST00000397746.7:c.403C= (FTCD) ENSP00000380854.3:p.Arg135=
ENST00000397748.5:c.403C= (FTCD) ENSP00000380856.1:p.Arg135=
ENST00000498355.6:n.472C= (FTCD)
XM_006723961.2:c.523C= (FTCD) XP_006724024.2:p.Arg175=
XM_006723961.4:c.523C= (FTCD) XP_006724024.2:p.Arg175=
XM_006723962.2:c.523C= (FTCD) XP_006724025.2:p.Arg175=
XM_006723962.4:c.523C= (FTCD) XP_006724025.2:p.Arg175=
XM_011529434.1:c.523C= (FTCD) XP_011527736.1:p.Arg175=
XM_011529434.3:c.523C= (FTCD) XP_011527736.1:p.Arg175=
XM_011529435.1:c.523C= (FTCD) XP_011527737.1:p.Arg175=
XM_011529435.3:c.523C= (FTCD) XP_011527737.1:p.Arg175=
XM_011529436.1:c.523C= (FTCD) XP_011527738.1:p.Arg175=
XM_011529436.3:c.523C= (FTCD) XP_011527738.1:p.Arg175=
XM_011529437.1:c.523C= (FTCD) XP_011527739.1:p.Arg175=
XM_011529437.3:c.523C= (FTCD) XP_011527739.1:p.Arg175=
XM_011529438.1:c.523C= (FTCD) XP_011527740.1:p.Arg175=
XM_011529439.1:c.10C= (FTCD) XP_011527741.1:p.Arg4=
XM_011529439.2:c.10C= (FTCD) XP_011527741.1:p.Arg4=
XM_011529440.1:c.523C= (FTCD) XP_011527742.1:p.Arg175=
XM_011529440.3:c.523C= (FTCD) XP_011527742.1:p.Arg175=
XR_937433.1:n.706C= (FTCD)
XR_937433.3:n.740C= (FTCD)