Canonical Allele Identifier: CA901505639

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• dbSNP Id: rs1321049691
• gnomAD v3: 3-160282635-A-G
• gnomAD v4: 3-160282635-A-G
• MyVariant Identifiers: chr3:g.160000423A>G (hg19) ; chr3:g.160282635A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282635A>G , CM000665.2:g.160282635A>G	GRCh38
NC_000003.11:g.160000423A>G , CM000665.1:g.160000423A>G	GRCh37
NC_000003.10:g.161483117A>G	NCBI36
NG_022932.1:g.121898T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-22T>C (IFT80) MANE Select	ENSP00000312778.7:n.1381-22T>C
ENST00000326448.11:c.1381-22T>C (IFT80)	ENSP00000312778.7:n.1381-22T>C
ENST00000483465.5:c.970-22T>C (IFT80)	ENSP00000418196.1:n.970-22T>C
ENST00000483754.1:c.1894-22T>C (TRIM59-IFT80)	ENSP00000456272.1:n.1894-22T>C
ENST00000487943.5:n.2600-22T>C (IFT80)
ENST00000496589.5:c.970-22T>C (IFT80)	ENSP00000420646.1:n.970-22T>C
NM_001190241.1:c.970-22T>C (IFT80)	NP_001177170.1:n.970-22T>C
NM_001190242.1:c.970-22T>C (IFT80)	NP_001177171.1:n.970-22T>C
NM_020800.2:c.1381-22T>C (IFT80)	NP_065851.1:n.1381-22T>C
XR_924138.1:n.2900-7037A>G (C3orf80)
NR_148401.1:n.2089-22T>C (TRIM59-IFT80)
NR_148402.1:n.3625-22T>C (TRIM59-IFT80)
NR_148403.1:n.3892-22T>C (TRIM59-IFT80)
NM_020800.3:c.1381-22T>C (IFT80) MANE Select	NP_065851.1:n.1381-22T>C
NM_001190241.2:c.970-22T>C (IFT80)	NP_001177170.1:n.970-22T>C
NM_001190242.2:c.970-22T>C (IFT80)	NP_001177171.1:n.970-22T>C