Canonical Allele Identifier: CA1365176084

Gene: RFT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53124143_53124146delinsAAGG , CM000665.2:g.53124143_53124146delinsAAGG	GRCh38
NC_000003.11:g.53158159_53158162delinsAAGG , CM000665.1:g.53158159_53158162delinsAAGG	GRCh37
NC_000003.10:g.53133199_53133202delinsAAGG	NCBI36
NG_009203.1:g.11309_11312delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-306_150-303delinsCCTT MANE Select	ENSP00000296292.3:n.150-306_150-303delinsCCTT
ENST00000296292.7:c.150-306_150-303delinsCCTT	ENSP00000296292.3:n.150-306_150-303delinsCCTT
ENST00000394738.7:c.150-1583_150-1580delinsCCTT	ENSP00000378223.3:n.150-1583_150-1580delinsCCTT
ENST00000467048.1:c.150-306_150-303delinsCCTT	ENSP00000420325.1:n.150-306_150-303delinsCCTT
NM_052859.3:c.150-306_150-303delinsCCTT	NP_443091.1:n.150-306_150-303delinsCCTT
XM_005265537.3:c.150-306_150-303delinsCCTT	XP_005265594.1:n.150-306_150-303delinsCCTT
XM_006713384.2:c.150-306_150-303delinsCCTT	XP_006713447.1:n.150-306_150-303delinsCCTT
XM_011534214.1:c.150-306_150-303delinsCCTT	XP_011532516.1:n.150-306_150-303delinsCCTT
XM_011534215.1:c.150-306_150-303delinsCCTT	XP_011532517.1:n.150-306_150-303delinsCCTT
XR_940507.1:n.209-306_209-303delinsCCTT
XM_005265537.4:c.150-306_150-303delinsCCTT	XP_005265594.1:n.150-306_150-303delinsCCTT
XM_006713384.3:c.150-306_150-303delinsCCTT	XP_006713447.1:n.150-306_150-303delinsCCTT
XM_011534214.2:c.150-306_150-303delinsCCTT	XP_011532516.1:n.150-306_150-303delinsCCTT
XM_011534215.3:c.150-306_150-303delinsCCTT	XP_011532517.1:n.150-306_150-303delinsCCTT
XM_011534216.3:c.-691-306_-691-303delinsCCTT	XP_011532518.1:n.-691-306_-691-303delinsCCTT
XM_017007460.1:c.150-306_150-303delinsCCTT	XP_016862949.1:n.150-306_150-303delinsCCTT
XM_017007461.2:c.-691-306_-691-303delinsCCTT	XP_016862950.1:n.-691-306_-691-303delinsCCTT
XR_001740360.2:n.216-306_216-303delinsCCTT
NM_052859.4:c.150-306_150-303delinsCCTT MANE Select	NP_443091.1:n.150-306_150-303delinsCCTT