Canonical Allele Identifier: CA2665424753
Gene: FYCO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45964331_45964332del , CM000665.2:g.45964331_45964332del GRCh38
NC_000003.11:g.46005823_46005824del , CM000665.1:g.46005823_46005824del GRCh37
NC_000003.10:g.45980827_45980828del NCBI36
NG_031955.1:g.36493_36494del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296137.7:c.3269+4_3269+5del MANE Select ENSP00000296137.2:n.3269+4_3269+5del
ENST00000296137.6:c.3269+4_3269+5del ENSP00000296137.2:n.3269+4_3269+5del
ENST00000535325.5:c.3269+4_3269+5del ENSP00000441178.1:n.3269+4_3269+5del
NM_024513.3:c.3269+4_3269+5del NP_078789.2:n.3269+4_3269+5del
XM_006713333.2:c.3269+4_3269+5del XP_006713396.1:n.3269+4_3269+5del
XM_006713334.2:c.3269+4_3269+5del XP_006713397.1:n.3269+4_3269+5del
XM_011534111.1:c.3269+4_3269+5del XP_011532413.1:n.3269+4_3269+5del
XM_011534112.1:c.3269+4_3269+5del XP_011532414.1:n.3269+4_3269+5del
XR_245157.1:n.3484+4_3484+5del
XM_006713333.3:c.3269+4_3269+5del XP_006713396.1:n.3269+4_3269+5del
XM_006713334.3:c.3269+4_3269+5del XP_006713397.1:n.3269+4_3269+5del
XM_011534111.3:c.3269+4_3269+5del XP_011532413.1:n.3269+4_3269+5del
XR_001740265.1:n.3365+701_3365+702del
NM_024513.4:c.3269+4_3269+5del MANE Select NP_078789.2:n.3269+4_3269+5del
NM_001386421.1:c.3269+4_3269+5del NP_001373350.1:n.3269+4_3269+5del
NM_001386422.1:c.3269+4_3269+5del NP_001373351.1:n.3269+4_3269+5del
NM_001386423.1:c.3269+4_3269+5del NP_001373352.1:n.3269+4_3269+5del
NM_001386424.1:c.3269+4_3269+5del NP_001373353.1:n.3269+4_3269+5del
NM_001386425.1:c.3269+4_3269+5del NP_001373354.1:n.3269+4_3269+5del
NM_001386426.1:c.3149+4_3149+5del NP_001373355.1:n.3149+4_3149+5del
NM_001386427.1:c.3125+4_3125+5del NP_001373356.1:n.3125+4_3125+5del
NM_001386428.1:c.3269+4_3269+5del NP_001373357.1:n.3269+4_3269+5del
NM_001386429.1:c.3269+4_3269+5del NP_001373358.1:n.3269+4_3269+5del
NM_001386430.1:c.2669+4_2669+5del NP_001373359.1:n.2669+4_2669+5del
NR_170107.1:n.3484+4_3484+5del