Canonical Allele Identifier: CA2666105034

Gene: RFT1

Linked Data

• gnomAD v4: 3-53123983-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123988del , CM000665.2:g.53123988del	GRCh38
NC_000003.11:g.53158004del , CM000665.1:g.53158004del	GRCh37
NC_000003.10:g.53133044del	NCBI36
NG_009203.1:g.11471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-144del MANE Select	ENSP00000296292.3:n.150-144del
ENST00000296292.7:c.150-144del	ENSP00000296292.3:n.150-144del
ENST00000394738.7:c.150-1421del	ENSP00000378223.3:n.150-1421del
ENST00000467048.1:c.150-144del	ENSP00000420325.1:n.150-144del
NM_052859.3:c.150-144del	NP_443091.1:n.150-144del
XM_005265537.3:c.150-144del	XP_005265594.1:n.150-144del
XM_006713384.2:c.150-144del	XP_006713447.1:n.150-144del
XM_011534214.1:c.150-144del	XP_011532516.1:n.150-144del
XM_011534215.1:c.150-144del	XP_011532517.1:n.150-144del
XR_940507.1:n.209-144del
XM_005265537.4:c.150-144del	XP_005265594.1:n.150-144del
XM_006713384.3:c.150-144del	XP_006713447.1:n.150-144del
XM_011534214.2:c.150-144del	XP_011532516.1:n.150-144del
XM_011534215.3:c.150-144del	XP_011532517.1:n.150-144del
XM_011534216.3:c.-691-144del	XP_011532518.1:n.-691-144del
XM_017007460.1:c.150-144del	XP_016862949.1:n.150-144del
XM_017007461.2:c.-691-144del	XP_016862950.1:n.-691-144del
XR_001740360.2:n.216-144del
NM_052859.4:c.150-144del MANE Select	NP_443091.1:n.150-144del