Canonical Allele Identifier: CA1365175932

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123835G= , CM000665.2:g.53123835G=	GRCh38
NC_000003.11:g.53157851G= , CM000665.1:g.53157851G=	GRCh37
NC_000003.10:g.53132891G=	NCBI36
NG_009203.1:g.11620C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.155C= MANE Select	ENSP00000296292.3:p.Thr52=
ENST00000296292.7:c.155C=	ENSP00000296292.3:p.Thr52=
ENST00000394738.7:c.150-1272C=	ENSP00000378223.3:n.150-1272C=
ENST00000467048.1:c.155C=	ENSP00000420325.1:p.Thr52=
NM_052859.3:c.155C=	NP_443091.1:p.Thr52=
XM_005265537.3:c.155C=	XP_005265594.1:p.Thr52=
XM_006713384.2:c.155C=	XP_006713447.1:p.Thr52=
XM_011534214.1:c.155C=	XP_011532516.1:p.Thr52=
XM_011534215.1:c.155C=	XP_011532517.1:p.Thr52=
XR_940507.1:n.214C=
XM_005265537.4:c.155C=	XP_005265594.1:p.Thr52=
XM_006713384.3:c.155C=	XP_006713447.1:p.Thr52=
XM_011534214.2:c.155C=	XP_011532516.1:p.Thr52=
XM_011534215.3:c.155C=	XP_011532517.1:p.Thr52=
XM_011534216.3:c.-686C=	XP_011532518.1:n.-686C=
XM_017007460.1:c.155C=	XP_016862949.1:p.Thr52=
XM_017007461.2:c.-686C=	XP_016862950.1:n.-686C=
XR_001740360.2:n.221C=
NM_052859.4:c.155C= MANE Select	NP_443091.1:p.Thr52=