Canonical Allele Identifier: CA2392525847
Gene: FTCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46150140C= , CM000683.2:g.46150140C= GRCh38
NC_000021.8:g.47570054C= , CM000683.1:g.47570054C= GRCh37
NC_000021.7:g.46394482C= NCBI36
NG_016191.1:g.10428G=

Transcript Alleles

HGVS Amino-acid change
ENST00000397746.8:c.885G= MANE Select ENSP00000380854.3:p.Glu295=
ENST00000291670.9:c.885G= ENSP00000291670.5:p.Glu295=
ENST00000397743.1:c.885G= ENSP00000380851.1:p.Glu295=
ENST00000397746.7:c.885G= ENSP00000380854.3:p.Glu295=
ENST00000397748.5:c.885G= ENSP00000380856.1:p.Glu295=
ENST00000498355.6:n.954G=
NM_006657.2:c.885G= NP_006648.1:p.Glu295=
NM_206965.1:c.885G= NP_996848.1:p.Glu295=
XM_006723961.2:c.1005G= XP_006724024.2:p.Glu335=
XM_006723962.2:c.1005G= XP_006724025.2:p.Glu335=
XM_011529434.1:c.1005G= XP_011527736.1:p.Glu335=
XM_011529435.1:c.1005G= XP_011527737.1:p.Glu335=
XM_011529436.1:c.1005G= XP_011527738.1:p.Glu335=
XM_011529437.1:c.1005G= XP_011527739.1:p.Glu335=
XM_011529438.1:c.1005G= XP_011527740.1:p.Glu335=
XM_011529439.1:c.492G= XP_011527741.1:p.Glu164=
XM_011529440.1:c.1005G= XP_011527742.1:p.Glu335=
XR_937433.1:n.1188G=
NM_001320412.1:c.885G= NP_001307341.1:p.Glu295=
XM_006723961.4:c.1005G= XP_006724024.2:p.Glu335=
XM_006723962.4:c.1005G= XP_006724025.2:p.Glu335=
XM_011529434.3:c.1005G= XP_011527736.1:p.Glu335=
XM_011529435.3:c.1005G= XP_011527737.1:p.Glu335=
XM_011529436.3:c.1005G= XP_011527738.1:p.Glu335=
XM_011529437.3:c.1005G= XP_011527739.1:p.Glu335=
XM_011529439.2:c.492G= XP_011527741.1:p.Glu164=
XM_011529440.3:c.1005G= XP_011527742.1:p.Glu335=
XR_937433.3:n.1222G=
NM_206965.2:c.885G= MANE Select NP_996848.1:p.Glu295=
NM_001320412.2:c.885G= NP_001307341.1:p.Glu295=
NM_006657.3:c.885G= NP_006648.1:p.Glu295=