Canonical Allele Identifier: CA2451519
Gene: RFT1 HGNC NCBI

Linked Data

dbSNP Id: rs771070006

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53123825del , CM000665.2:g.53123825del GRCh38
NC_000003.11:g.53157841del , CM000665.1:g.53157841del GRCh37
NC_000003.10:g.53132881del NCBI36
NG_009203.1:g.11630del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296292.8:c.165del MANE Select ENSP00000296292.3:p.Ser56GlnfsTer?
ENST00000296292.7:c.165del ENSP00000296292.3:p.Ser56GlnfsTer?
ENST00000394738.7:c.150-1262del ENSP00000378223.3:n.150-1262del
ENST00000467048.1:c.165del ENSP00000420325.1:p.Ser56GlnfsTer?
NM_052859.3:c.165del NP_443091.1:p.Ser56GlnfsTer?
XM_005265537.3:c.165del XP_005265594.1:p.Ser56GlnfsTer?
XM_006713384.2:c.165del XP_006713447.1:p.Ser56GlnfsTer?
XM_011534214.1:c.165del XP_011532516.1:p.Ser56GlnfsTer?
XM_011534215.1:c.165del XP_011532517.1:p.Ser56GlnfsTer?
XR_940507.1:n.224del
XM_005265537.4:c.165del XP_005265594.1:p.Ser56GlnfsTer?
XM_006713384.3:c.165del XP_006713447.1:p.Ser56GlnfsTer?
XM_011534214.2:c.165del XP_011532516.1:p.Ser56GlnfsTer?
XM_011534215.3:c.165del XP_011532517.1:p.Ser56GlnfsTer?
XM_011534216.3:c.-676del XP_011532518.1:n.-676del
XM_017007460.1:c.165del XP_016862949.1:p.Ser56GlnfsTer?
XM_017007461.2:c.-676del XP_016862950.1:n.-676del
XR_001740360.2:n.231del
NM_052859.4:c.165del MANE Select NP_443091.1:p.Ser56GlnfsTer?