Canonical Allele Identifier: CA410559061

Gene: FTCD

Linked Data

• MyVariant Identifiers: chr21:g.47558503C>T (hg19) ; chr21:g.46138589C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138589C>T , CM000683.2:g.46138589C>T	GRCh38
NC_000021.8:g.47558503C>T , CM000683.1:g.47558503C>T	GRCh37
NC_000021.7:g.46382931C>T	NCBI36
NG_016191.1:g.21979G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000460011.6:c.-103G>A	ENSP00000507070.1:n.-103G>A
ENST00000494498.2:c.96G>A	ENSP00000507847.1:p.Leu32=
ENST00000397746.8:c.1362G>A MANE Select	ENSP00000380854.3:p.Leu454=
ENST00000291670.9:c.1362G>A	ENSP00000291670.5:p.Leu454=
ENST00000397743.1:c.1318G>A	ENSP00000380851.1:p.Gly440Ser
ENST00000397746.7:c.1362G>A	ENSP00000380854.3:p.Leu454=
ENST00000397748.5:c.1362G>A	ENSP00000380856.1:p.Leu454=
ENST00000460011.5:n.691G>A
ENST00000488577.1:n.388G>A
ENST00000494498.1:n.663G>A
ENST00000498355.6:n.1431G>A
NM_006657.2:c.1362G>A	NP_006648.1:p.Leu454=
NM_206965.1:c.1362G>A	NP_996848.1:p.Leu454=
XM_006723961.2:c.1611G>A	XP_006724024.2:p.Leu537=
XM_006723962.2:c.1611G>A	XP_006724025.2:p.Leu537=
XM_011529434.1:c.1611G>A	XP_011527736.1:p.Leu537=
XM_011529435.1:c.1482G>A	XP_011527737.1:p.Leu494=
XM_011529436.1:c.1611G>A	XP_011527738.1:p.Leu537=
XM_011529437.1:c.1611G>A	XP_011527739.1:p.Leu537=
XM_011529438.1:c.1482G>A	XP_011527740.1:p.Leu494=
XM_011529439.1:c.1098G>A	XP_011527741.1:p.Leu366=
XR_937433.1:n.1794G>A
NM_001320412.1:c.1362G>A	NP_001307341.1:p.Leu454=
XM_006723961.4:c.1611G>A	XP_006724024.2:p.Leu537=
XM_006723962.4:c.1611G>A	XP_006724025.2:p.Leu537=
XM_011529434.3:c.1611G>A	XP_011527736.1:p.Leu537=
XM_011529435.3:c.1482G>A	XP_011527737.1:p.Leu494=
XM_011529436.3:c.1611G>A	XP_011527738.1:p.Leu537=
XM_011529437.3:c.1611G>A	XP_011527739.1:p.Leu537=
XM_011529439.2:c.1098G>A	XP_011527741.1:p.Leu366=
XR_937433.3:n.1828G>A
NM_206965.2:c.1362G>A MANE Select	NP_996848.1:p.Leu454=
NM_001320412.2:c.1362G>A	NP_001307341.1:p.Leu454=
NM_006657.3:c.1362G>A	NP_006648.1:p.Leu454=