Canonical Allele Identifier: CA1415115658
Gene: IFT80 HGNC NCBI
TRIM59-IFT80 HGNC NCBI
C3orf80 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160282841_160282842delinsTA , CM000665.2:g.160282841_160282842delinsTA GRCh38
NC_000003.11:g.160000629_160000630delinsTA , CM000665.1:g.160000629_160000630delinsTA GRCh37
NC_000003.10:g.161483323_161483324delinsTA NCBI36
NG_022932.1:g.121691_121692delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000326448.12:c.1381-229_1381-228delinsTA (IFT80) MANE Select ENSP00000312778.7:n.1381-229_1381-228delinsTA
ENST00000326448.11:c.1381-229_1381-228delinsTA (IFT80) ENSP00000312778.7:n.1381-229_1381-228delinsTA
ENST00000483465.5:c.970-229_970-228delinsTA (IFT80) ENSP00000418196.1:n.970-229_970-228delinsTA
ENST00000483754.1:c.1894-229_1894-228delinsTA (TRIM59-IFT80) ENSP00000456272.1:n.1894-229_1894-228delinsTA
ENST00000487943.5:n.2600-229_2600-228delinsTA (IFT80)
ENST00000496589.5:c.970-229_970-228delinsTA (IFT80) ENSP00000420646.1:n.970-229_970-228delinsTA
NM_001190241.1:c.970-229_970-228delinsTA (IFT80) NP_001177170.1:n.970-229_970-228delinsTA
NM_001190242.1:c.970-229_970-228delinsTA (IFT80) NP_001177171.1:n.970-229_970-228delinsTA
NM_020800.2:c.1381-229_1381-228delinsTA (IFT80) NP_065851.1:n.1381-229_1381-228delinsTA
XR_924138.1:n.2900-6831_2900-6830delinsTA (C3orf80)
NR_148401.1:n.2089-229_2089-228delinsTA (TRIM59-IFT80)
NR_148402.1:n.3625-229_3625-228delinsTA (TRIM59-IFT80)
NR_148403.1:n.3892-229_3892-228delinsTA (TRIM59-IFT80)
NM_020800.3:c.1381-229_1381-228delinsTA (IFT80) MANE Select NP_065851.1:n.1381-229_1381-228delinsTA
NM_001190241.2:c.970-229_970-228delinsTA (IFT80) NP_001177170.1:n.970-229_970-228delinsTA
NM_001190242.2:c.970-229_970-228delinsTA (IFT80) NP_001177171.1:n.970-229_970-228delinsTA