Canonical Allele Identifier: CA749855891

Gene: FTCD

Linked Data

• dbSNP Id: rs1230625772
• MyVariant Identifiers: chr21:g.47558572_47558576del (hg19) ; chr21:g.46138658_46138662del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138658_46138662del , CM000683.2:g.46138658_46138662del	GRCh38
NC_000021.8:g.47558572_47558576del , CM000683.1:g.47558572_47558576del	GRCh37
NC_000021.7:g.46383000_46383004del	NCBI36
NG_016191.1:g.21906_21910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-16_-160-12del	ENSP00000507070.1:n.-160-16_-160-12del
ENST00000494498.2:c.39-16_39-12del	ENSP00000507847.1:n.39-16_39-12del
ENST00000397746.8:c.1305-16_1305-12del MANE Select	ENSP00000380854.3:n.1305-16_1305-12del
ENST00000291670.9:c.1305-16_1305-12del	ENSP00000291670.5:n.1305-16_1305-12del
ENST00000397743.1:c.1261-16_1261-12del	ENSP00000380851.1:n.1261-16_1261-12del
ENST00000397746.7:c.1305-16_1305-12del	ENSP00000380854.3:n.1305-16_1305-12del
ENST00000397748.5:c.1305-16_1305-12del	ENSP00000380856.1:n.1305-16_1305-12del
ENST00000460011.5:n.634-16_634-12del
ENST00000488577.1:n.331-16_331-12del
ENST00000494498.1:n.606-16_606-12del
ENST00000498355.6:n.1374-16_1374-12del
NM_006657.2:c.1305-16_1305-12del	NP_006648.1:n.1305-16_1305-12del
NM_206965.1:c.1305-16_1305-12del	NP_996848.1:n.1305-16_1305-12del
XM_006723961.2:c.1554-16_1554-12del	XP_006724024.2:n.1554-16_1554-12del
XM_006723962.2:c.1554-16_1554-12del	XP_006724025.2:n.1554-16_1554-12del
XM_011529434.1:c.1554-16_1554-12del	XP_011527736.1:n.1554-16_1554-12del
XM_011529435.1:c.1425-16_1425-12del	XP_011527737.1:n.1425-16_1425-12del
XM_011529436.1:c.1554-16_1554-12del	XP_011527738.1:n.1554-16_1554-12del
XM_011529437.1:c.1554-16_1554-12del	XP_011527739.1:n.1554-16_1554-12del
XM_011529438.1:c.1425-16_1425-12del	XP_011527740.1:n.1425-16_1425-12del
XM_011529439.1:c.1041-16_1041-12del	XP_011527741.1:n.1041-16_1041-12del
XR_937433.1:n.1737-16_1737-12del
NM_001320412.1:c.1305-16_1305-12del	NP_001307341.1:n.1305-16_1305-12del
XM_006723961.4:c.1554-16_1554-12del	XP_006724024.2:n.1554-16_1554-12del
XM_006723962.4:c.1554-16_1554-12del	XP_006724025.2:n.1554-16_1554-12del
XM_011529434.3:c.1554-16_1554-12del	XP_011527736.1:n.1554-16_1554-12del
XM_011529435.3:c.1425-16_1425-12del	XP_011527737.1:n.1425-16_1425-12del
XM_011529436.3:c.1554-16_1554-12del	XP_011527738.1:n.1554-16_1554-12del
XM_011529437.3:c.1554-16_1554-12del	XP_011527739.1:n.1554-16_1554-12del
XM_011529439.2:c.1041-16_1041-12del	XP_011527741.1:n.1041-16_1041-12del
XR_937433.3:n.1771-16_1771-12del
NM_206965.2:c.1305-16_1305-12del MANE Select	NP_996848.1:n.1305-16_1305-12del
NM_001320412.2:c.1305-16_1305-12del	NP_001307341.1:n.1305-16_1305-12del
NM_006657.3:c.1305-16_1305-12del	NP_006648.1:n.1305-16_1305-12del