Canonical Allele Identifier: CA1365175886
Gene: RFT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53123724G= , CM000665.2:g.53123724G= GRCh38
NC_000003.11:g.53157740G= , CM000665.1:g.53157740G= GRCh37
NC_000003.10:g.53132780G= NCBI36
NG_009203.1:g.11731C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296292.8:c.266C= MANE Select ENSP00000296292.3:p.Thr89=
ENST00000296292.7:c.266C= ENSP00000296292.3:p.Thr89=
ENST00000394738.7:c.150-1161C= ENSP00000378223.3:n.150-1161C=
ENST00000467048.1:c.266C= ENSP00000420325.1:p.Thr89=
NM_052859.3:c.266C= NP_443091.1:p.Thr89=
XM_005265537.3:c.266C= XP_005265594.1:p.Thr89=
XM_006713384.2:c.266C= XP_006713447.1:p.Thr89=
XM_011534214.1:c.266C= XP_011532516.1:p.Thr89=
XM_011534215.1:c.266C= XP_011532517.1:p.Thr89=
XR_940507.1:n.325C=
XM_005265537.4:c.266C= XP_005265594.1:p.Thr89=
XM_006713384.3:c.266C= XP_006713447.1:p.Thr89=
XM_011534214.2:c.266C= XP_011532516.1:p.Thr89=
XM_011534215.3:c.266C= XP_011532517.1:p.Thr89=
XM_011534216.3:c.-575C= XP_011532518.1:n.-575C=
XM_017007460.1:c.266C= XP_016862949.1:p.Thr89=
XM_017007461.2:c.-575C= XP_016862950.1:n.-575C=
XR_001740360.2:n.332C=
NM_052859.4:c.266C= MANE Select NP_443091.1:p.Thr89=