Canonical Allele Identifier: CA1365175887
Gene: RFT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53123726T= , CM000665.2:g.53123726T= GRCh38
NC_000003.11:g.53157742T= , CM000665.1:g.53157742T= GRCh37
NC_000003.10:g.53132782T= NCBI36
NG_009203.1:g.11729A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296292.8:c.264A= MANE Select ENSP00000296292.3:p.Leu88=
ENST00000296292.7:c.264A= ENSP00000296292.3:p.Leu88=
ENST00000394738.7:c.150-1163A= ENSP00000378223.3:n.150-1163A=
ENST00000467048.1:c.264A= ENSP00000420325.1:p.Leu88=
NM_052859.3:c.264A= NP_443091.1:p.Leu88=
XM_005265537.3:c.264A= XP_005265594.1:p.Leu88=
XM_006713384.2:c.264A= XP_006713447.1:p.Leu88=
XM_011534214.1:c.264A= XP_011532516.1:p.Leu88=
XM_011534215.1:c.264A= XP_011532517.1:p.Leu88=
XR_940507.1:n.323A=
XM_005265537.4:c.264A= XP_005265594.1:p.Leu88=
XM_006713384.3:c.264A= XP_006713447.1:p.Leu88=
XM_011534214.2:c.264A= XP_011532516.1:p.Leu88=
XM_011534215.3:c.264A= XP_011532517.1:p.Leu88=
XM_011534216.3:c.-577A= XP_011532518.1:n.-577A=
XM_017007460.1:c.264A= XP_016862949.1:p.Leu88=
XM_017007461.2:c.-577A= XP_016862950.1:n.-577A=
XR_001740360.2:n.330A=
NM_052859.4:c.264A= MANE Select NP_443091.1:p.Leu88=