Canonical Allele Identifier: CA1365175927

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123824_53123825delinsAG , CM000665.2:g.53123824_53123825delinsAG	GRCh38
NC_000003.11:g.53157840_53157841delinsAG , CM000665.1:g.53157840_53157841delinsAG	GRCh37
NC_000003.10:g.53132880_53132881delinsAG	NCBI36
NG_009203.1:g.11630_11631delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.165_166delinsCT MANE Select	ENSP00000296292.3:p.Tyr55=
ENST00000296292.7:c.165_166delinsCT	ENSP00000296292.3:p.Tyr55=
ENST00000394738.7:c.150-1262_150-1261delinsCT	ENSP00000378223.3:n.150-1262_150-1261delinsCT
ENST00000467048.1:c.165_166delinsCT	ENSP00000420325.1:p.Tyr55=
NM_052859.3:c.165_166delinsCT	NP_443091.1:p.Tyr55=
XM_005265537.3:c.165_166delinsCT	XP_005265594.1:p.Tyr55=
XM_006713384.2:c.165_166delinsCT	XP_006713447.1:p.Tyr55=
XM_011534214.1:c.165_166delinsCT	XP_011532516.1:p.Tyr55=
XM_011534215.1:c.165_166delinsCT	XP_011532517.1:p.Tyr55=
XR_940507.1:n.224_225delinsCT
XM_005265537.4:c.165_166delinsCT	XP_005265594.1:p.Tyr55=
XM_006713384.3:c.165_166delinsCT	XP_006713447.1:p.Tyr55=
XM_011534214.2:c.165_166delinsCT	XP_011532516.1:p.Tyr55=
XM_011534215.3:c.165_166delinsCT	XP_011532517.1:p.Tyr55=
XM_011534216.3:c.-676_-675delinsCT	XP_011532518.1:n.-676_-675delinsCT
XM_017007460.1:c.165_166delinsCT	XP_016862949.1:p.Tyr55=
XM_017007461.2:c.-676_-675delinsCT	XP_016862950.1:n.-676_-675delinsCT
XR_001740360.2:n.231_232delinsCT
NM_052859.4:c.165_166delinsCT MANE Select	NP_443091.1:p.Tyr55=