Canonical Allele Identifier: CA1365175977
Gene: RFT1 HGNC NCBI

Linked Data

dbSNP Id: rs1702039520

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53123920A>C , CM000665.2:g.53123920A>C GRCh38
NC_000003.11:g.53157936A>C , CM000665.1:g.53157936A>C GRCh37
NC_000003.10:g.53132976A>C NCBI36
NG_009203.1:g.11535T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296292.8:c.150-80T>G MANE Select ENSP00000296292.3:n.150-80T>G
ENST00000296292.7:c.150-80T>G ENSP00000296292.3:n.150-80T>G
ENST00000394738.7:c.150-1357T>G ENSP00000378223.3:n.150-1357T>G
ENST00000467048.1:c.150-80T>G ENSP00000420325.1:n.150-80T>G
NM_052859.3:c.150-80T>G NP_443091.1:n.150-80T>G
XM_005265537.3:c.150-80T>G XP_005265594.1:n.150-80T>G
XM_006713384.2:c.150-80T>G XP_006713447.1:n.150-80T>G
XM_011534214.1:c.150-80T>G XP_011532516.1:n.150-80T>G
XM_011534215.1:c.150-80T>G XP_011532517.1:n.150-80T>G
XR_940507.1:n.209-80T>G
XM_005265537.4:c.150-80T>G XP_005265594.1:n.150-80T>G
XM_006713384.3:c.150-80T>G XP_006713447.1:n.150-80T>G
XM_011534214.2:c.150-80T>G XP_011532516.1:n.150-80T>G
XM_011534215.3:c.150-80T>G XP_011532517.1:n.150-80T>G
XM_011534216.3:c.-691-80T>G XP_011532518.1:n.-691-80T>G
XM_017007460.1:c.150-80T>G XP_016862949.1:n.150-80T>G
XM_017007461.2:c.-691-80T>G XP_016862950.1:n.-691-80T>G
XR_001740360.2:n.216-80T>G
NM_052859.4:c.150-80T>G MANE Select NP_443091.1:n.150-80T>G