Canonical Allele Identifier: CA645609799

Gene: FTCD

Linked Data

• COSMIC: COSM5347592 ; COSM5347593

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46138626_46138658del , CM000683.2:g.46138626_46138658del	GRCh38
NC_000021.8:g.47558540_47558572del , CM000683.1:g.47558540_47558572del	GRCh37
NC_000021.7:g.46382968_46383000del	NCBI36
NG_016191.1:g.21910_21942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460011.6:c.-160-12_-140del
ENST00000494498.2:c.39-12_59del
ENST00000397746.8:c.1305-12_1325del
ENST00000291670.9:c.1305-12_1325del
ENST00000397743.1:c.1261-12_1281del
ENST00000397746.7:c.1305-12_1325del
ENST00000397748.5:c.1305-12_1325del
ENST00000460011.5:n.634-12_654del
ENST00000488577.1:n.331-12_351del
ENST00000494498.1:n.606-12_626del
ENST00000498355.6:n.1374-12_1394del
NM_006657.2:c.1305-12_1325del
NM_206965.1:c.1305-12_1325del
XM_006723961.2:c.1554-12_1574del
XM_006723962.2:c.1554-12_1574del
XM_011529434.1:c.1554-12_1574del
XM_011529435.1:c.1425-12_1445del
XM_011529436.1:c.1554-12_1574del
XM_011529437.1:c.1554-12_1574del
XM_011529438.1:c.1425-12_1445del
XM_011529439.1:c.1041-12_1061del
XR_937433.1:n.1737-12_1757del
NM_001320412.1:c.1305-12_1325del
XM_006723961.4:c.1554-12_1574del
XM_006723962.4:c.1554-12_1574del
XM_011529434.3:c.1554-12_1574del
XM_011529435.3:c.1425-12_1445del
XM_011529436.3:c.1554-12_1574del
XM_011529437.3:c.1554-12_1574del
XM_011529439.2:c.1041-12_1061del
XR_937433.3:n.1771-12_1791del
NM_206965.2:c.1305-12_1325del
NM_001320412.2:c.1305-12_1325del
NM_006657.3:c.1305-12_1325del