Canonical Allele Identifier: CA1365176128

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53124212_53124214delinsCCT , CM000665.2:g.53124212_53124214delinsCCT	GRCh38
NC_000003.11:g.53158228_53158230delinsCCT , CM000665.1:g.53158228_53158230delinsCCT	GRCh37
NC_000003.10:g.53133268_53133270delinsCCT	NCBI36
NG_009203.1:g.11241_11243delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-374_150-372delinsAGG MANE Select	ENSP00000296292.3:n.150-374_150-372delinsAGG
ENST00000296292.7:c.150-374_150-372delinsAGG	ENSP00000296292.3:n.150-374_150-372delinsAGG
ENST00000394738.7:c.150-1651_150-1649delinsAGG	ENSP00000378223.3:n.150-1651_150-1649delinsAGG
ENST00000467048.1:c.150-374_150-372delinsAGG	ENSP00000420325.1:n.150-374_150-372delinsAGG
NM_052859.3:c.150-374_150-372delinsAGG	NP_443091.1:n.150-374_150-372delinsAGG
XM_005265537.3:c.150-374_150-372delinsAGG	XP_005265594.1:n.150-374_150-372delinsAGG
XM_006713384.2:c.150-374_150-372delinsAGG	XP_006713447.1:n.150-374_150-372delinsAGG
XM_011534214.1:c.150-374_150-372delinsAGG	XP_011532516.1:n.150-374_150-372delinsAGG
XM_011534215.1:c.150-374_150-372delinsAGG	XP_011532517.1:n.150-374_150-372delinsAGG
XR_940507.1:n.209-374_209-372delinsAGG
XM_005265537.4:c.150-374_150-372delinsAGG	XP_005265594.1:n.150-374_150-372delinsAGG
XM_006713384.3:c.150-374_150-372delinsAGG	XP_006713447.1:n.150-374_150-372delinsAGG
XM_011534214.2:c.150-374_150-372delinsAGG	XP_011532516.1:n.150-374_150-372delinsAGG
XM_011534215.3:c.150-374_150-372delinsAGG	XP_011532517.1:n.150-374_150-372delinsAGG
XM_011534216.3:c.-691-374_-691-372delinsAGG	XP_011532518.1:n.-691-374_-691-372delinsAGG
XM_017007460.1:c.150-374_150-372delinsAGG	XP_016862949.1:n.150-374_150-372delinsAGG
XM_017007461.2:c.-691-374_-691-372delinsAGG	XP_016862950.1:n.-691-374_-691-372delinsAGG
XR_001740360.2:n.216-374_216-372delinsAGG
NM_052859.4:c.150-374_150-372delinsAGG MANE Select	NP_443091.1:n.150-374_150-372delinsAGG