Canonical Allele Identifier: CA2666104936

Gene: RFT1

Linked Data

• gnomAD v4: 3-53123672-GCTCACTACACCTGCCTTCCTGAAACGTGTCTCCTGCCAAAGCACAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123678_53123723del , CM000665.2:g.53123678_53123723del	GRCh38
NC_000003.11:g.53157694_53157739del , CM000665.1:g.53157694_53157739del	GRCh37
NC_000003.10:g.53132734_53132779del	NCBI36
NG_009203.1:g.11737_11782del

Transcript Alleles

HGVS	Amino-acid change
ENST00000296292.8:c.266+6_266+51del MANE Select	ENSP00000296292.3:n.266+6_266+51del
ENST00000296292.7:c.266+6_266+51del	ENSP00000296292.3:n.266+6_266+51del
ENST00000394738.7:c.150-1155_150-1110del	ENSP00000378223.3:n.150-1155_150-1110del
ENST00000467048.1:c.266+6_266+51del	ENSP00000420325.1:n.266+6_266+51del
NM_052859.3:c.266+6_266+51del	NP_443091.1:n.266+6_266+51del
XM_005265537.3:c.266+6_266+51del	XP_005265594.1:n.266+6_266+51del
XM_006713384.2:c.266+6_266+51del	XP_006713447.1:n.266+6_266+51del
XM_011534214.1:c.266+6_266+51del	XP_011532516.1:n.266+6_266+51del
XM_011534215.1:c.266+6_266+51del	XP_011532517.1:n.266+6_266+51del
XR_940507.1:n.325+6_325+51del
XM_005265537.4:c.266+6_266+51del	XP_005265594.1:n.266+6_266+51del
XM_006713384.3:c.266+6_266+51del	XP_006713447.1:n.266+6_266+51del
XM_011534214.2:c.266+6_266+51del	XP_011532516.1:n.266+6_266+51del
XM_011534215.3:c.266+6_266+51del	XP_011532517.1:n.266+6_266+51del
XM_011534216.3:c.-575+6_-575+51del	XP_011532518.1:n.-575+6_-575+51del
XM_017007460.1:c.266+6_266+51del	XP_016862949.1:n.266+6_266+51del
XM_017007461.2:c.-575+6_-575+51del	XP_016862950.1:n.-575+6_-575+51del
XR_001740360.2:n.332+6_332+51del
NM_052859.4:c.266+6_266+51del MANE Select	NP_443091.1:n.266+6_266+51del