Canonical Allele Identifier: CA410558475
Gene: FTCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46138513G>C , CM000683.2:g.46138513G>C GRCh38
NC_000021.8:g.47558427G>C , CM000683.1:g.47558427G>C GRCh37
NC_000021.7:g.46382855G>C NCBI36
NG_016191.1:g.22055C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000460011.6:c.-27C>G ENSP00000507070.1:n.-27C>G
ENST00000494498.2:c.172C>G ENSP00000507847.1:p.Leu58Val
ENST00000397746.8:c.1438C>G MANE Select ENSP00000380854.3:p.Leu480Val
ENST00000291670.9:c.1438C>G ENSP00000291670.5:p.Leu480Val
ENST00000397743.1:c.1394C>G ENSP00000380851.1:p.Pro465Arg
ENST00000397746.7:c.1438C>G ENSP00000380854.3:p.Leu480Val
ENST00000397748.5:c.1438C>G ENSP00000380856.1:p.Leu480Val
ENST00000446405.5:c.60C>G
ENST00000460011.5:n.767C>G
ENST00000494498.1:n.739C>G
ENST00000498355.6:n.1507C>G
NM_006657.2:c.1438C>G NP_006648.1:p.Leu480Val
NM_206965.1:c.1438C>G NP_996848.1:p.Leu480Val
XM_006723961.2:c.1687C>G XP_006724024.2:p.Leu563Val
XM_006723962.2:c.1687C>G XP_006724025.2:p.Leu563Val
XM_011529434.1:c.1687C>G XP_011527736.1:p.Leu563Val
XM_011529435.1:c.1558C>G XP_011527737.1:p.Leu520Val
XM_011529436.1:c.1687C>G XP_011527738.1:p.Leu563Val
XM_011529437.1:c.1687C>G XP_011527739.1:p.Leu563Val
XM_011529438.1:c.1558C>G XP_011527740.1:p.Leu520Val
XM_011529439.1:c.1174C>G XP_011527741.1:p.Leu392Val
XR_937433.1:n.1870C>G
NM_001320412.1:c.1438C>G NP_001307341.1:p.Leu480Val
XM_006723961.4:c.1687C>G XP_006724024.2:p.Leu563Val
XM_006723962.4:c.1687C>G XP_006724025.2:p.Leu563Val
XM_011529434.3:c.1687C>G XP_011527736.1:p.Leu563Val
XM_011529435.3:c.1558C>G XP_011527737.1:p.Leu520Val
XM_011529436.3:c.1687C>G XP_011527738.1:p.Leu563Val
XM_011529437.3:c.1687C>G XP_011527739.1:p.Leu563Val
XM_011529439.2:c.1174C>G XP_011527741.1:p.Leu392Val
XR_937433.3:n.1904C>G
NM_206965.2:c.1438C>G MANE Select NP_996848.1:p.Leu480Val
NM_001320412.2:c.1438C>G NP_001307341.1:p.Leu480Val
NM_006657.3:c.1438C>G NP_006648.1:p.Leu480Val