Canonical Allele Identifier: CA1365175909

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123790C= , CM000665.2:g.53123790C=	GRCh38
NC_000003.11:g.53157806C= , CM000665.1:g.53157806C=	GRCh37
NC_000003.10:g.53132846C=	NCBI36
NG_009203.1:g.11665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.200G= MANE Select	ENSP00000296292.3:p.Arg67=
ENST00000296292.7:c.200G=	ENSP00000296292.3:p.Arg67=
ENST00000394738.7:c.150-1227G=	ENSP00000378223.3:n.150-1227G=
ENST00000467048.1:c.200G=	ENSP00000420325.1:p.Arg67=
NM_052859.3:c.200G=	NP_443091.1:p.Arg67=
XM_005265537.3:c.200G=	XP_005265594.1:p.Arg67=
XM_006713384.2:c.200G=	XP_006713447.1:p.Arg67=
XM_011534214.1:c.200G=	XP_011532516.1:p.Arg67=
XM_011534215.1:c.200G=	XP_011532517.1:p.Arg67=
XR_940507.1:n.259G=
XM_005265537.4:c.200G=	XP_005265594.1:p.Arg67=
XM_006713384.3:c.200G=	XP_006713447.1:p.Arg67=
XM_011534214.2:c.200G=	XP_011532516.1:p.Arg67=
XM_011534215.3:c.200G=	XP_011532517.1:p.Arg67=
XM_011534216.3:c.-641G=	XP_011532518.1:n.-641G=
XM_017007460.1:c.200G=	XP_016862949.1:p.Arg67=
XM_017007461.2:c.-641G=	XP_016862950.1:n.-641G=
XR_001740360.2:n.266G=
NM_052859.4:c.200G= MANE Select	NP_443091.1:p.Arg67=