Canonical Allele Identifier: CA1365176088

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53124149_53124152delinsGAGA , CM000665.2:g.53124149_53124152delinsGAGA	GRCh38
NC_000003.11:g.53158165_53158168delinsGAGA , CM000665.1:g.53158165_53158168delinsGAGA	GRCh37
NC_000003.10:g.53133205_53133208delinsGAGA	NCBI36
NG_009203.1:g.11303_11306delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-312_150-309delinsTCTC MANE Select	ENSP00000296292.3:n.150-312_150-309delinsTCTC
ENST00000296292.7:c.150-312_150-309delinsTCTC	ENSP00000296292.3:n.150-312_150-309delinsTCTC
ENST00000394738.7:c.150-1589_150-1586delinsTCTC	ENSP00000378223.3:n.150-1589_150-1586delinsTCTC
ENST00000467048.1:c.150-312_150-309delinsTCTC	ENSP00000420325.1:n.150-312_150-309delinsTCTC
NM_052859.3:c.150-312_150-309delinsTCTC	NP_443091.1:n.150-312_150-309delinsTCTC
XM_005265537.3:c.150-312_150-309delinsTCTC	XP_005265594.1:n.150-312_150-309delinsTCTC
XM_006713384.2:c.150-312_150-309delinsTCTC	XP_006713447.1:n.150-312_150-309delinsTCTC
XM_011534214.1:c.150-312_150-309delinsTCTC	XP_011532516.1:n.150-312_150-309delinsTCTC
XM_011534215.1:c.150-312_150-309delinsTCTC	XP_011532517.1:n.150-312_150-309delinsTCTC
XR_940507.1:n.209-312_209-309delinsTCTC
XM_005265537.4:c.150-312_150-309delinsTCTC	XP_005265594.1:n.150-312_150-309delinsTCTC
XM_006713384.3:c.150-312_150-309delinsTCTC	XP_006713447.1:n.150-312_150-309delinsTCTC
XM_011534214.2:c.150-312_150-309delinsTCTC	XP_011532516.1:n.150-312_150-309delinsTCTC
XM_011534215.3:c.150-312_150-309delinsTCTC	XP_011532517.1:n.150-312_150-309delinsTCTC
XM_011534216.3:c.-691-312_-691-309delinsTCTC	XP_011532518.1:n.-691-312_-691-309delinsTCTC
XM_017007460.1:c.150-312_150-309delinsTCTC	XP_016862949.1:n.150-312_150-309delinsTCTC
XM_017007461.2:c.-691-312_-691-309delinsTCTC	XP_016862950.1:n.-691-312_-691-309delinsTCTC
XR_001740360.2:n.216-312_216-309delinsTCTC
NM_052859.4:c.150-312_150-309delinsTCTC MANE Select	NP_443091.1:n.150-312_150-309delinsTCTC