Canonical Allele Identifier: CA2759121212

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282639_160282640insACG , CM000665.2:g.160282639_160282640insACG	GRCh38
NC_000003.11:g.160000427_160000428insACG , CM000665.1:g.160000427_160000428insACG	GRCh37
NC_000003.10:g.161483121_161483122insACG	NCBI36
NG_022932.1:g.121893_121894insCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-27_1381-26insCGT (IFT80) MANE Select	ENSP00000312778.7:n.1381-27_1381-26insCGT
ENST00000326448.11:c.1381-27_1381-26insCGT (IFT80)	ENSP00000312778.7:n.1381-27_1381-26insCGT
ENST00000483465.5:c.970-27_970-26insCGT (IFT80)	ENSP00000418196.1:n.970-27_970-26insCGT
ENST00000483754.1:c.1894-27_1894-26insCGT (TRIM59-IFT80)	ENSP00000456272.1:n.1894-27_1894-26insCGT
ENST00000487943.5:n.2600-27_2600-26insCGT (IFT80)
ENST00000496589.5:c.970-27_970-26insCGT (IFT80)	ENSP00000420646.1:n.970-27_970-26insCGT
NM_001190241.1:c.970-27_970-26insCGT (IFT80)	NP_001177170.1:n.970-27_970-26insCGT
NM_001190242.1:c.970-27_970-26insCGT (IFT80)	NP_001177171.1:n.970-27_970-26insCGT
NM_020800.2:c.1381-27_1381-26insCGT (IFT80)	NP_065851.1:n.1381-27_1381-26insCGT
XR_924138.1:n.2900-7033_2900-7032insACG (C3orf80)
NR_148401.1:n.2089-27_2089-26insCGT (TRIM59-IFT80)
NR_148402.1:n.3625-27_3625-26insCGT (TRIM59-IFT80)
NR_148403.1:n.3892-27_3892-26insCGT (TRIM59-IFT80)
NM_020800.3:c.1381-27_1381-26insCGT (IFT80) MANE Select	NP_065851.1:n.1381-27_1381-26insCGT
NM_001190241.2:c.970-27_970-26insCGT (IFT80)	NP_001177170.1:n.970-27_970-26insCGT
NM_001190242.2:c.970-27_970-26insCGT (IFT80)	NP_001177171.1:n.970-27_970-26insCGT