Canonical Allele Identifier: CA410559435
Gene: FTCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46138630G>A , CM000683.2:g.46138630G>A GRCh38
NC_000021.8:g.47558544G>A , CM000683.1:g.47558544G>A GRCh37
NC_000021.7:g.46382972G>A NCBI36
NG_016191.1:g.21938C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000460011.6:c.-144C>T ENSP00000507070.1:n.-144C>T
ENST00000494498.2:c.55C>T ENSP00000507847.1:p.Gln19Ter
ENST00000397746.8:c.1321C>T MANE Select ENSP00000380854.3:p.Gln441Ter
ENST00000291670.9:c.1321C>T ENSP00000291670.5:p.Gln441Ter
ENST00000397743.1:c.1277C>T ENSP00000380851.1:p.Thr426Ile
ENST00000397746.7:c.1321C>T ENSP00000380854.3:p.Gln441Ter
ENST00000397748.5:c.1321C>T ENSP00000380856.1:p.Gln441Ter
ENST00000460011.5:n.650C>T
ENST00000488577.1:n.347C>T
ENST00000494498.1:n.622C>T
ENST00000498355.6:n.1390C>T
NM_006657.2:c.1321C>T NP_006648.1:p.Gln441Ter
NM_206965.1:c.1321C>T NP_996848.1:p.Gln441Ter
XM_006723961.2:c.1570C>T XP_006724024.2:p.Gln524Ter
XM_006723962.2:c.1570C>T XP_006724025.2:p.Gln524Ter
XM_011529434.1:c.1570C>T XP_011527736.1:p.Gln524Ter
XM_011529435.1:c.1441C>T XP_011527737.1:p.Gln481Ter
XM_011529436.1:c.1570C>T XP_011527738.1:p.Gln524Ter
XM_011529437.1:c.1570C>T XP_011527739.1:p.Gln524Ter
XM_011529438.1:c.1441C>T XP_011527740.1:p.Gln481Ter
XM_011529439.1:c.1057C>T XP_011527741.1:p.Gln353Ter
XR_937433.1:n.1753C>T
NM_001320412.1:c.1321C>T NP_001307341.1:p.Gln441Ter
XM_006723961.4:c.1570C>T XP_006724024.2:p.Gln524Ter
XM_006723962.4:c.1570C>T XP_006724025.2:p.Gln524Ter
XM_011529434.3:c.1570C>T XP_011527736.1:p.Gln524Ter
XM_011529435.3:c.1441C>T XP_011527737.1:p.Gln481Ter
XM_011529436.3:c.1570C>T XP_011527738.1:p.Gln524Ter
XM_011529437.3:c.1570C>T XP_011527739.1:p.Gln524Ter
XM_011529439.2:c.1057C>T XP_011527741.1:p.Gln353Ter
XR_937433.3:n.1787C>T
NM_206965.2:c.1321C>T MANE Select NP_996848.1:p.Gln441Ter
NM_001320412.2:c.1321C>T NP_001307341.1:p.Gln441Ter
NM_006657.3:c.1321C>T NP_006648.1:p.Gln441Ter