Canonical Allele Identifier: CA749855593

Gene: FTCD

Linked Data

• dbSNP Id: rs1446412026
• gnomAD v3: 21-46138465-CTGCTTTGCGGCAGGAG-C
• gnomAD v4: 21-46138465-CTGCTTTGCGGCAGGAG-C
• MyVariant Identifiers: chr21:g.47558380_47558395del (hg19) ; chr21:g.46138466_46138481del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138466_46138481del , CM000683.2:g.46138466_46138481del	GRCh38
NC_000021.8:g.47558380_47558395del , CM000683.1:g.47558380_47558395del	GRCh37
NC_000021.7:g.46382808_46382823del	NCBI36
NG_016191.1:g.22087_22102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-22+27_-22+42del	ENSP00000507070.1:n.-22+27_-22+42del
ENST00000494498.2:c.177+27_177+42del	ENSP00000507847.1:n.177+27_177+42del
ENST00000397746.8:c.1443+27_1443+42del MANE Select	ENSP00000380854.3:n.1443+27_1443+42del
ENST00000291670.9:c.1443+27_1443+42del	ENSP00000291670.5:n.1443+27_1443+42del
ENST00000397743.1:c.1399+27_1399+42del	ENSP00000380851.1:n.1399+27_1399+42del
ENST00000397746.7:c.1443+27_1443+42del	ENSP00000380854.3:n.1443+27_1443+42del
ENST00000397748.5:c.1443+27_1443+42del	ENSP00000380856.1:n.1443+27_1443+42del
ENST00000446405.5:c.65+27_65+42del
ENST00000460011.5:n.772+27_772+42del
ENST00000494498.1:n.744+27_744+42del
ENST00000498355.6:n.1512+27_1512+42del
NM_006657.2:c.1443+27_1443+42del	NP_006648.1:n.1443+27_1443+42del
NM_206965.1:c.1443+27_1443+42del	NP_996848.1:n.1443+27_1443+42del
XM_006723961.2:c.1692+27_1692+42del	XP_006724024.2:n.1692+27_1692+42del
XM_006723962.2:c.1692+27_1692+42del	XP_006724025.2:n.1692+27_1692+42del
XM_011529434.1:c.1692+27_1692+42del	XP_011527736.1:n.1692+27_1692+42del
XM_011529435.1:c.1563+27_1563+42del	XP_011527737.1:n.1563+27_1563+42del
XM_011529436.1:c.1692+27_1692+42del	XP_011527738.1:n.1692+27_1692+42del
XM_011529437.1:c.1692+27_1692+42del	XP_011527739.1:n.1692+27_1692+42del
XM_011529438.1:c.1563+27_1563+42del	XP_011527740.1:n.1563+27_1563+42del
XM_011529439.1:c.1179+27_1179+42del	XP_011527741.1:n.1179+27_1179+42del
XR_937433.1:n.1875+27_1875+42del
NM_001320412.1:c.1443+27_1443+42del	NP_001307341.1:n.1443+27_1443+42del
XM_006723961.4:c.1692+27_1692+42del	XP_006724024.2:n.1692+27_1692+42del
XM_006723962.4:c.1692+27_1692+42del	XP_006724025.2:n.1692+27_1692+42del
XM_011529434.3:c.1692+27_1692+42del	XP_011527736.1:n.1692+27_1692+42del
XM_011529435.3:c.1563+27_1563+42del	XP_011527737.1:n.1563+27_1563+42del
XM_011529436.3:c.1692+27_1692+42del	XP_011527738.1:n.1692+27_1692+42del
XM_011529437.3:c.1692+27_1692+42del	XP_011527739.1:n.1692+27_1692+42del
XM_011529439.2:c.1179+27_1179+42del	XP_011527741.1:n.1179+27_1179+42del
XR_937433.3:n.1909+27_1909+42del
NM_206965.2:c.1443+27_1443+42del MANE Select	NP_996848.1:n.1443+27_1443+42del
NM_001320412.2:c.1443+27_1443+42del	NP_001307341.1:n.1443+27_1443+42del
NM_006657.3:c.1443+27_1443+42del	NP_006648.1:n.1443+27_1443+42del