Canonical Allele Identifier: CA1365175943

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53123857_53123858delinsGA , CM000665.2:g.53123857_53123858delinsGA	GRCh38
NC_000003.11:g.53157873_53157874delinsGA , CM000665.1:g.53157873_53157874delinsGA	GRCh37
NC_000003.10:g.53132913_53132914delinsGA	NCBI36
NG_009203.1:g.11597_11598delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-18_150-17delinsTC MANE Select	ENSP00000296292.3:n.150-18_150-17delinsTC
ENST00000296292.7:c.150-18_150-17delinsTC	ENSP00000296292.3:n.150-18_150-17delinsTC
ENST00000394738.7:c.150-1295_150-1294delinsTC	ENSP00000378223.3:n.150-1295_150-1294delinsTC
ENST00000467048.1:c.150-18_150-17delinsTC	ENSP00000420325.1:n.150-18_150-17delinsTC
NM_052859.3:c.150-18_150-17delinsTC	NP_443091.1:n.150-18_150-17delinsTC
XM_005265537.3:c.150-18_150-17delinsTC	XP_005265594.1:n.150-18_150-17delinsTC
XM_006713384.2:c.150-18_150-17delinsTC	XP_006713447.1:n.150-18_150-17delinsTC
XM_011534214.1:c.150-18_150-17delinsTC	XP_011532516.1:n.150-18_150-17delinsTC
XM_011534215.1:c.150-18_150-17delinsTC	XP_011532517.1:n.150-18_150-17delinsTC
XR_940507.1:n.209-18_209-17delinsTC
XM_005265537.4:c.150-18_150-17delinsTC	XP_005265594.1:n.150-18_150-17delinsTC
XM_006713384.3:c.150-18_150-17delinsTC	XP_006713447.1:n.150-18_150-17delinsTC
XM_011534214.2:c.150-18_150-17delinsTC	XP_011532516.1:n.150-18_150-17delinsTC
XM_011534215.3:c.150-18_150-17delinsTC	XP_011532517.1:n.150-18_150-17delinsTC
XM_011534216.3:c.-691-18_-691-17delinsTC	XP_011532518.1:n.-691-18_-691-17delinsTC
XM_017007460.1:c.150-18_150-17delinsTC	XP_016862949.1:n.150-18_150-17delinsTC
XM_017007461.2:c.-691-18_-691-17delinsTC	XP_016862950.1:n.-691-18_-691-17delinsTC
XR_001740360.2:n.216-18_216-17delinsTC
NM_052859.4:c.150-18_150-17delinsTC MANE Select	NP_443091.1:n.150-18_150-17delinsTC