Canonical Allele Identifier: CA1415115145
Gene: IFT80 HGNC NCBI
TRIM59-IFT80 HGNC NCBI
C3orf80 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160282400_160282404delinsGATTC , CM000665.2:g.160282400_160282404delinsGATTC GRCh38
NC_000003.11:g.160000188_160000192delinsGATTC , CM000665.1:g.160000188_160000192delinsGATTC GRCh37
NC_000003.10:g.161482882_161482886delinsGATTC NCBI36
NG_022932.1:g.122129_122133delinsGAATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000326448.12:c.1516+74_1516+78delinsGAATC (IFT80) MANE Select ENSP00000312778.7:n.1516+74_1516+78delinsGAATC
ENST00000326448.11:c.1516+74_1516+78delinsGAATC (IFT80) ENSP00000312778.7:n.1516+74_1516+78delinsGAATC
ENST00000483465.5:c.1105+74_1105+78delinsGAATC (IFT80) ENSP00000418196.1:n.1105+74_1105+78delinsGAATC
ENST00000483754.1:c.2029+74_2029+78delinsGAATC (TRIM59-IFT80) ENSP00000456272.1:n.2029+74_2029+78delinsGAATC
ENST00000487943.5:n.2735+74_2735+78delinsGAATC (IFT80)
ENST00000496589.5:c.1105+74_1105+78delinsGAATC (IFT80) ENSP00000420646.1:n.1105+74_1105+78delinsGAATC
NM_001190241.1:c.1105+74_1105+78delinsGAATC (IFT80) NP_001177170.1:n.1105+74_1105+78delinsGAATC
NM_001190242.1:c.1105+74_1105+78delinsGAATC (IFT80) NP_001177171.1:n.1105+74_1105+78delinsGAATC
NM_020800.2:c.1516+74_1516+78delinsGAATC (IFT80) NP_065851.1:n.1516+74_1516+78delinsGAATC
XR_924138.1:n.2900-7272_2900-7268delinsGATTC (C3orf80)
NR_148401.1:n.2224+74_2224+78delinsGAATC (TRIM59-IFT80)
NR_148402.1:n.3760+74_3760+78delinsGAATC (TRIM59-IFT80)
NR_148403.1:n.4027+74_4027+78delinsGAATC (TRIM59-IFT80)
NM_020800.3:c.1516+74_1516+78delinsGAATC (IFT80) MANE Select NP_065851.1:n.1516+74_1516+78delinsGAATC
NM_001190241.2:c.1105+74_1105+78delinsGAATC (IFT80) NP_001177170.1:n.1105+74_1105+78delinsGAATC
NM_001190242.2:c.1105+74_1105+78delinsGAATC (IFT80) NP_001177171.1:n.1105+74_1105+78delinsGAATC