Canonical Allele Identifier: CA1365175896

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123755A= , CM000665.2:g.53123755A=	GRCh38
NC_000003.11:g.53157771A= , CM000665.1:g.53157771A=	GRCh37
NC_000003.10:g.53132811A=	NCBI36
NG_009203.1:g.11700T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.235T= MANE Select	ENSP00000296292.3:p.Trp79=
ENST00000296292.7:c.235T=	ENSP00000296292.3:p.Trp79=
ENST00000394738.7:c.150-1192T=	ENSP00000378223.3:n.150-1192T=
ENST00000467048.1:c.235T=	ENSP00000420325.1:p.Trp79=
NM_052859.3:c.235T=	NP_443091.1:p.Trp79=
XM_005265537.3:c.235T=	XP_005265594.1:p.Trp79=
XM_006713384.2:c.235T=	XP_006713447.1:p.Trp79=
XM_011534214.1:c.235T=	XP_011532516.1:p.Trp79=
XM_011534215.1:c.235T=	XP_011532517.1:p.Trp79=
XR_940507.1:n.294T=
XM_005265537.4:c.235T=	XP_005265594.1:p.Trp79=
XM_006713384.3:c.235T=	XP_006713447.1:p.Trp79=
XM_011534214.2:c.235T=	XP_011532516.1:p.Trp79=
XM_011534215.3:c.235T=	XP_011532517.1:p.Trp79=
XM_011534216.3:c.-606T=	XP_011532518.1:n.-606T=
XM_017007460.1:c.235T=	XP_016862949.1:p.Trp79=
XM_017007461.2:c.-606T=	XP_016862950.1:n.-606T=
XR_001740360.2:n.301T=
NM_052859.4:c.235T= MANE Select	NP_443091.1:p.Trp79=