Canonical Allele Identifier: CA1365175816

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123530_53123531delinsTC , CM000665.2:g.53123530_53123531delinsTC	GRCh38
NC_000003.11:g.53157546_53157547delinsTC , CM000665.1:g.53157546_53157547delinsTC	GRCh37
NC_000003.10:g.53132586_53132587delinsTC	NCBI36
NG_009203.1:g.11924_11925delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.266+193_266+194delinsGA MANE Select	ENSP00000296292.3:n.266+193_266+194delinsGA
ENST00000296292.7:c.266+193_266+194delinsGA	ENSP00000296292.3:n.266+193_266+194delinsGA
ENST00000394738.7:c.150-968_150-967delinsGA	ENSP00000378223.3:n.150-968_150-967delinsGA
ENST00000467048.1:c.266+193_266+194delinsGA	ENSP00000420325.1:n.266+193_266+194delinsGA
NM_052859.3:c.266+193_266+194delinsGA	NP_443091.1:n.266+193_266+194delinsGA
XM_005265537.3:c.266+193_266+194delinsGA	XP_005265594.1:n.266+193_266+194delinsGA
XM_006713384.2:c.266+193_266+194delinsGA	XP_006713447.1:n.266+193_266+194delinsGA
XM_011534214.1:c.266+193_266+194delinsGA	XP_011532516.1:n.266+193_266+194delinsGA
XM_011534215.1:c.266+193_266+194delinsGA	XP_011532517.1:n.266+193_266+194delinsGA
XR_940507.1:n.325+193_325+194delinsGA
XM_005265537.4:c.266+193_266+194delinsGA	XP_005265594.1:n.266+193_266+194delinsGA
XM_006713384.3:c.266+193_266+194delinsGA	XP_006713447.1:n.266+193_266+194delinsGA
XM_011534214.2:c.266+193_266+194delinsGA	XP_011532516.1:n.266+193_266+194delinsGA
XM_011534215.3:c.266+193_266+194delinsGA	XP_011532517.1:n.266+193_266+194delinsGA
XM_011534216.3:c.-575+193_-575+194delinsGA	XP_011532518.1:n.-575+193_-575+194delinsGA
XM_017007460.1:c.266+193_266+194delinsGA	XP_016862949.1:n.266+193_266+194delinsGA
XM_017007461.2:c.-575+193_-575+194delinsGA	XP_016862950.1:n.-575+193_-575+194delinsGA
XR_001740360.2:n.332+193_332+194delinsGA
NM_052859.4:c.266+193_266+194delinsGA MANE Select	NP_443091.1:n.266+193_266+194delinsGA