Canonical Allele Identifier: CA2353527
Gene: FYCO1 HGNC NCBI

Linked Data

dbSNP Id: rs746947148

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45979672_45979674del , CM000665.2:g.45979672_45979674del GRCh38
NC_000003.11:g.46021164_46021166del , CM000665.1:g.46021164_46021166del GRCh37
NC_000003.10:g.45996168_45996170del NCBI36
NG_031955.1:g.21154_21156del

Transcript Alleles

HGVS Amino-acid change
ENST00000296137.7:c.288+34_288+36del MANE Select ENSP00000296137.2:n.288+34_288+36del
ENST00000296137.6:c.288+34_288+36del ENSP00000296137.2:n.288+34_288+36del
ENST00000535325.5:c.288+34_288+36del ENSP00000441178.1:n.288+34_288+36del
NM_024513.3:c.288+34_288+36del NP_078789.2:n.288+34_288+36del
XM_006713333.2:c.288+34_288+36del XP_006713396.1:n.288+34_288+36del
XM_006713334.2:c.288+34_288+36del XP_006713397.1:n.288+34_288+36del
XM_011534111.1:c.288+34_288+36del XP_011532413.1:n.288+34_288+36del
XM_011534112.1:c.288+34_288+36del XP_011532414.1:n.288+34_288+36del
XR_245157.1:n.503+34_503+36del
XM_006713333.3:c.288+34_288+36del XP_006713396.1:n.288+34_288+36del
XM_006713334.3:c.288+34_288+36del XP_006713397.1:n.288+34_288+36del
XM_011534111.3:c.288+34_288+36del XP_011532413.1:n.288+34_288+36del
XR_001740265.1:n.503+34_503+36del
NM_024513.4:c.288+34_288+36del MANE Select NP_078789.2:n.288+34_288+36del
NM_001386421.1:c.288+34_288+36del NP_001373350.1:n.288+34_288+36del
NM_001386422.1:c.288+34_288+36del NP_001373351.1:n.288+34_288+36del
NM_001386423.1:c.288+34_288+36del NP_001373352.1:n.288+34_288+36del
NM_001386424.1:c.288+34_288+36del NP_001373353.1:n.288+34_288+36del
NM_001386425.1:c.288+34_288+36del NP_001373354.1:n.288+34_288+36del
NM_001386426.1:c.168+34_168+36del NP_001373355.1:n.168+34_168+36del
NM_001386427.1:c.288+34_288+36del NP_001373356.1:n.288+34_288+36del
NM_001386428.1:c.288+34_288+36del NP_001373357.1:n.288+34_288+36del
NM_001386429.1:c.288+34_288+36del NP_001373358.1:n.288+34_288+36del
NM_001386430.1:c.-62+5185_-62+5187del NP_001373359.1:n.-62+5185_-62+5187del
NR_170107.1:n.503+34_503+36del