Canonical Allele Identifier: CA2392518426
Gene: FTCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46138490_46138491delinsTC , CM000683.2:g.46138490_46138491delinsTC GRCh38
NC_000021.8:g.47558404_47558405delinsTC , CM000683.1:g.47558404_47558405delinsTC GRCh37
NC_000021.7:g.46382832_46382833delinsTC NCBI36
NG_016191.1:g.22077_22078delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000460011.6:c.-22+17_-22+18delinsGA ENSP00000507070.1:n.-22+17_-22+18delinsGA
ENST00000494498.2:c.177+17_177+18delinsGA ENSP00000507847.1:n.177+17_177+18delinsGA
ENST00000397746.8:c.1443+17_1443+18delinsGA MANE Select ENSP00000380854.3:n.1443+17_1443+18delinsGA
ENST00000291670.9:c.1443+17_1443+18delinsGA ENSP00000291670.5:n.1443+17_1443+18delinsGA
ENST00000397743.1:c.1399+17_1399+18delinsGA ENSP00000380851.1:n.1399+17_1399+18delinsGA
ENST00000397746.7:c.1443+17_1443+18delinsGA ENSP00000380854.3:n.1443+17_1443+18delinsGA
ENST00000397748.5:c.1443+17_1443+18delinsGA ENSP00000380856.1:n.1443+17_1443+18delinsGA
ENST00000446405.5:c.65+17_65+18delinsGA
ENST00000460011.5:n.772+17_772+18delinsGA
ENST00000494498.1:n.744+17_744+18delinsGA
ENST00000498355.6:n.1512+17_1512+18delinsGA
NM_006657.2:c.1443+17_1443+18delinsGA NP_006648.1:n.1443+17_1443+18delinsGA
NM_206965.1:c.1443+17_1443+18delinsGA NP_996848.1:n.1443+17_1443+18delinsGA
XM_006723961.2:c.1692+17_1692+18delinsGA XP_006724024.2:n.1692+17_1692+18delinsGA
XM_006723962.2:c.1692+17_1692+18delinsGA XP_006724025.2:n.1692+17_1692+18delinsGA
XM_011529434.1:c.1692+17_1692+18delinsGA XP_011527736.1:n.1692+17_1692+18delinsGA
XM_011529435.1:c.1563+17_1563+18delinsGA XP_011527737.1:n.1563+17_1563+18delinsGA
XM_011529436.1:c.1692+17_1692+18delinsGA XP_011527738.1:n.1692+17_1692+18delinsGA
XM_011529437.1:c.1692+17_1692+18delinsGA XP_011527739.1:n.1692+17_1692+18delinsGA
XM_011529438.1:c.1563+17_1563+18delinsGA XP_011527740.1:n.1563+17_1563+18delinsGA
XM_011529439.1:c.1179+17_1179+18delinsGA XP_011527741.1:n.1179+17_1179+18delinsGA
XR_937433.1:n.1875+17_1875+18delinsGA
NM_001320412.1:c.1443+17_1443+18delinsGA NP_001307341.1:n.1443+17_1443+18delinsGA
XM_006723961.4:c.1692+17_1692+18delinsGA XP_006724024.2:n.1692+17_1692+18delinsGA
XM_006723962.4:c.1692+17_1692+18delinsGA XP_006724025.2:n.1692+17_1692+18delinsGA
XM_011529434.3:c.1692+17_1692+18delinsGA XP_011527736.1:n.1692+17_1692+18delinsGA
XM_011529435.3:c.1563+17_1563+18delinsGA XP_011527737.1:n.1563+17_1563+18delinsGA
XM_011529436.3:c.1692+17_1692+18delinsGA XP_011527738.1:n.1692+17_1692+18delinsGA
XM_011529437.3:c.1692+17_1692+18delinsGA XP_011527739.1:n.1692+17_1692+18delinsGA
XM_011529439.2:c.1179+17_1179+18delinsGA XP_011527741.1:n.1179+17_1179+18delinsGA
XR_937433.3:n.1909+17_1909+18delinsGA
NM_206965.2:c.1443+17_1443+18delinsGA MANE Select NP_996848.1:n.1443+17_1443+18delinsGA
NM_001320412.2:c.1443+17_1443+18delinsGA NP_001307341.1:n.1443+17_1443+18delinsGA
NM_006657.3:c.1443+17_1443+18delinsGA NP_006648.1:n.1443+17_1443+18delinsGA