Canonical Allele Identifier: CA2654977145

Gene: FTCD

Linked Data

• gnomAD v4: 21-46138611-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138613_46138614dup , CM000683.2:g.46138613_46138614dup	GRCh38
NC_000021.8:g.47558527_47558528dup , CM000683.1:g.47558527_47558528dup	GRCh37
NC_000021.7:g.46382955_46382956dup	NCBI36
NG_016191.1:g.21955_21956dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-127_-126dup	ENSP00000507070.1:n.-127_-126dup
ENST00000494498.2:c.72_73dup	ENSP00000507847.1:p.Ala25GlyfsTer7
ENST00000397746.8:c.1338_1339dup MANE Select	ENSP00000380854.3:p.Ala447GlyfsTer7
ENST00000291670.9:c.1338_1339dup	ENSP00000291670.5:p.Ala447GlyfsTer7
ENST00000397743.1:c.1294_1295dup	ENSP00000380851.1:p.Ser433AlafsTer?
ENST00000397746.7:c.1338_1339dup	ENSP00000380854.3:p.Ala447GlyfsTer7
ENST00000397748.5:c.1338_1339dup	ENSP00000380856.1:p.Ala447GlyfsTer7
ENST00000460011.5:n.667_668dup
ENST00000488577.1:n.364_365dup
ENST00000494498.1:n.639_640dup
ENST00000498355.6:n.1407_1408dup
NM_006657.2:c.1338_1339dup	NP_006648.1:p.Ala447GlyfsTer7
NM_206965.1:c.1338_1339dup	NP_996848.1:p.Ala447GlyfsTer7
XM_006723961.2:c.1587_1588dup	XP_006724024.2:p.Ala530GlyfsTer7
XM_006723962.2:c.1587_1588dup	XP_006724025.2:p.Ala530GlyfsTer7
XM_011529434.1:c.1587_1588dup	XP_011527736.1:p.Ala530GlyfsTer7
XM_011529435.1:c.1458_1459dup	XP_011527737.1:p.Ala487GlyfsTer7
XM_011529436.1:c.1587_1588dup	XP_011527738.1:p.Ala530GlyfsTer7
XM_011529437.1:c.1587_1588dup	XP_011527739.1:p.Ala530GlyfsTer7
XM_011529438.1:c.1458_1459dup	XP_011527740.1:p.Ala487GlyfsTer7
XM_011529439.1:c.1074_1075dup	XP_011527741.1:p.Ala359GlyfsTer7
XR_937433.1:n.1770_1771dup
NM_001320412.1:c.1338_1339dup	NP_001307341.1:p.Ala447GlyfsTer7
XM_006723961.4:c.1587_1588dup	XP_006724024.2:p.Ala530GlyfsTer7
XM_006723962.4:c.1587_1588dup	XP_006724025.2:p.Ala530GlyfsTer7
XM_011529434.3:c.1587_1588dup	XP_011527736.1:p.Ala530GlyfsTer7
XM_011529435.3:c.1458_1459dup	XP_011527737.1:p.Ala487GlyfsTer7
XM_011529436.3:c.1587_1588dup	XP_011527738.1:p.Ala530GlyfsTer7
XM_011529437.3:c.1587_1588dup	XP_011527739.1:p.Ala530GlyfsTer7
XM_011529439.2:c.1074_1075dup	XP_011527741.1:p.Ala359GlyfsTer7
XR_937433.3:n.1804_1805dup
NM_206965.2:c.1338_1339dup MANE Select	NP_996848.1:p.Ala447GlyfsTer7
NM_001320412.2:c.1338_1339dup	NP_001307341.1:p.Ala447GlyfsTer7
NM_006657.3:c.1338_1339dup	NP_006648.1:p.Ala447GlyfsTer7