Canonical Allele Identifier: CA2685152
Gene: IFT80 HGNC NCBI
TRIM59-IFT80 HGNC NCBI
C3orf80 HGNC NCBI

Linked Data

dbSNP Id: rs762561295

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160282579C>T , CM000665.2:g.160282579C>T GRCh38
NC_000003.11:g.160000367C>T , CM000665.1:g.160000367C>T GRCh37
NC_000003.10:g.161483061C>T NCBI36
NG_022932.1:g.121954G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000326448.12:c.1415G>A (IFT80) MANE Select ENSP00000312778.7:p.Gly472Glu
ENST00000326448.11:c.1415G>A (IFT80) ENSP00000312778.7:p.Gly472Glu
ENST00000483465.5:c.1004G>A (IFT80) ENSP00000418196.1:p.Gly335Glu
ENST00000483754.1:c.1928G>A (TRIM59-IFT80) ENSP00000456272.1:p.Gly643Glu
ENST00000487943.5:n.2634G>A (IFT80)
ENST00000496589.5:c.1004G>A (IFT80) ENSP00000420646.1:p.Gly335Glu
NM_001190241.1:c.1004G>A (IFT80) NP_001177170.1:p.Gly335Glu
NM_001190242.1:c.1004G>A (IFT80) NP_001177171.1:p.Gly335Glu
NM_020800.2:c.1415G>A (IFT80) NP_065851.1:p.Gly472Glu
XR_924138.1:n.2900-7093C>T (C3orf80)
NR_148401.1:n.2123G>A (TRIM59-IFT80)
NR_148402.1:n.3659G>A (TRIM59-IFT80)
NR_148403.1:n.3926G>A (TRIM59-IFT80)
NM_020800.3:c.1415G>A (IFT80) MANE Select NP_065851.1:p.Gly472Glu
NM_001190241.2:c.1004G>A (IFT80) NP_001177170.1:p.Gly335Glu
NM_001190242.2:c.1004G>A (IFT80) NP_001177171.1:p.Gly335Glu