Canonical Allele Identifier: CA1365176103

Gene: RFT1

Linked Data

• dbSNP Id: rs1702047095

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53124167_53124168del , CM000665.2:g.53124167_53124168del	GRCh38
NC_000003.11:g.53158183_53158184del , CM000665.1:g.53158183_53158184del	GRCh37
NC_000003.10:g.53133223_53133224del	NCBI36
NG_009203.1:g.11289_11290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-326_150-325del MANE Select	ENSP00000296292.3:n.150-326_150-325del
ENST00000296292.7:c.150-326_150-325del	ENSP00000296292.3:n.150-326_150-325del
ENST00000394738.7:c.150-1603_150-1602del	ENSP00000378223.3:n.150-1603_150-1602del
ENST00000467048.1:c.150-326_150-325del	ENSP00000420325.1:n.150-326_150-325del
NM_052859.3:c.150-326_150-325del	NP_443091.1:n.150-326_150-325del
XM_005265537.3:c.150-326_150-325del	XP_005265594.1:n.150-326_150-325del
XM_006713384.2:c.150-326_150-325del	XP_006713447.1:n.150-326_150-325del
XM_011534214.1:c.150-326_150-325del	XP_011532516.1:n.150-326_150-325del
XM_011534215.1:c.150-326_150-325del	XP_011532517.1:n.150-326_150-325del
XR_940507.1:n.209-326_209-325del
XM_005265537.4:c.150-326_150-325del	XP_005265594.1:n.150-326_150-325del
XM_006713384.3:c.150-326_150-325del	XP_006713447.1:n.150-326_150-325del
XM_011534214.2:c.150-326_150-325del	XP_011532516.1:n.150-326_150-325del
XM_011534215.3:c.150-326_150-325del	XP_011532517.1:n.150-326_150-325del
XM_011534216.3:c.-691-326_-691-325del	XP_011532518.1:n.-691-326_-691-325del
XM_017007460.1:c.150-326_150-325del	XP_016862949.1:n.150-326_150-325del
XM_017007461.2:c.-691-326_-691-325del	XP_016862950.1:n.-691-326_-691-325del
XR_001740360.2:n.216-326_216-325del
NM_052859.4:c.150-326_150-325del MANE Select	NP_443091.1:n.150-326_150-325del