Canonical Allele Identifier: CA10073938

Gene: FTCD FTCD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46151997C>T , CM000683.2:g.46151997C>T	GRCh38
NC_000021.8:g.47571911C>T , CM000683.1:g.47571911C>T	GRCh37
NC_000021.7:g.46396339C>T	NCBI36
NG_016191.1:g.8571G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397746.8:c.368-17G>A (FTCD) MANE Select	ENSP00000380854.3:n.368-17G>A
ENST00000291670.9:c.368-17G>A (FTCD)	ENSP00000291670.5:n.368-17G>A
ENST00000397743.1:c.368-17G>A (FTCD)	ENSP00000380851.1:n.368-17G>A
ENST00000397746.7:c.368-17G>A (FTCD)	ENSP00000380854.3:n.368-17G>A
ENST00000397748.5:c.368-17G>A (FTCD)	ENSP00000380856.1:n.368-17G>A
ENST00000498355.6:n.420G>A (FTCD)
NM_006657.2:c.368-17G>A (FTCD)	NP_006648.1:n.368-17G>A
NM_206965.1:c.368-17G>A (FTCD)	NP_996848.1:n.368-17G>A
XM_006723961.2:c.488-17G>A (FTCD)	XP_006724024.2:n.488-17G>A
XM_006723962.2:c.488-17G>A (FTCD)	XP_006724025.2:n.488-17G>A
XM_011529434.1:c.488-17G>A (FTCD)	XP_011527736.1:n.488-17G>A
XM_011529435.1:c.488-17G>A (FTCD)	XP_011527737.1:n.488-17G>A
XM_011529436.1:c.488-17G>A (FTCD)	XP_011527738.1:n.488-17G>A
XM_011529437.1:c.488-17G>A (FTCD)	XP_011527739.1:n.488-17G>A
XM_011529438.1:c.488-17G>A (FTCD)	XP_011527740.1:n.488-17G>A
XM_011529439.1:c.-43G>A (FTCD)	XP_011527741.1:n.-43G>A
XM_011529440.1:c.488-17G>A (FTCD)	XP_011527742.1:n.488-17G>A
XR_937433.1:n.671-17G>A (FTCD)
NM_001320412.1:c.368-17G>A (FTCD)	NP_001307341.1:n.368-17G>A
NM_001350598.1:c.225+238C>T (FTCD-AS1)	NP_001337527.1:n.225+238C>T
XM_006723961.4:c.488-17G>A (FTCD)	XP_006724024.2:n.488-17G>A
XM_006723962.4:c.488-17G>A (FTCD)	XP_006724025.2:n.488-17G>A
XM_011529434.3:c.488-17G>A (FTCD)	XP_011527736.1:n.488-17G>A
XM_011529435.3:c.488-17G>A (FTCD)	XP_011527737.1:n.488-17G>A
XM_011529436.3:c.488-17G>A (FTCD)	XP_011527738.1:n.488-17G>A
XM_011529437.3:c.488-17G>A (FTCD)	XP_011527739.1:n.488-17G>A
XM_011529439.2:c.-43G>A (FTCD)	XP_011527741.1:n.-43G>A
XM_011529440.3:c.488-17G>A (FTCD)	XP_011527742.1:n.488-17G>A
XR_937433.3:n.705-17G>A (FTCD)
NM_206965.2:c.368-17G>A (FTCD) MANE Select	NP_996848.1:n.368-17G>A
NM_001320412.2:c.368-17G>A (FTCD)	NP_001307341.1:n.368-17G>A
NM_006657.3:c.368-17G>A (FTCD)	NP_006648.1:n.368-17G>A
NR_170989.1:n.146+238C>T (FTCD-AS1)