Canonical Allele Identifier: CA2759121245

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282673_160282674insAG , CM000665.2:g.160282673_160282674insAG	GRCh38
NC_000003.11:g.160000461_160000462insAG , CM000665.1:g.160000461_160000462insAG	GRCh37
NC_000003.10:g.161483155_161483156insAG	NCBI36
NG_022932.1:g.121859_121860insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-61_1381-60insCT (IFT80) MANE Select	ENSP00000312778.7:n.1381-61_1381-60insCT
ENST00000326448.11:c.1381-61_1381-60insCT (IFT80)	ENSP00000312778.7:n.1381-61_1381-60insCT
ENST00000483465.5:c.970-61_970-60insCT (IFT80)	ENSP00000418196.1:n.970-61_970-60insCT
ENST00000483754.1:c.1894-61_1894-60insCT (TRIM59-IFT80)	ENSP00000456272.1:n.1894-61_1894-60insCT
ENST00000487943.5:n.2600-61_2600-60insCT (IFT80)
ENST00000496589.5:c.970-61_970-60insCT (IFT80)	ENSP00000420646.1:n.970-61_970-60insCT
NM_001190241.1:c.970-61_970-60insCT (IFT80)	NP_001177170.1:n.970-61_970-60insCT
NM_001190242.1:c.970-61_970-60insCT (IFT80)	NP_001177171.1:n.970-61_970-60insCT
NM_020800.2:c.1381-61_1381-60insCT (IFT80)	NP_065851.1:n.1381-61_1381-60insCT
XR_924138.1:n.2900-6999_2900-6998insAG (C3orf80)
NR_148401.1:n.2089-61_2089-60insCT (TRIM59-IFT80)
NR_148402.1:n.3625-61_3625-60insCT (TRIM59-IFT80)
NR_148403.1:n.3892-61_3892-60insCT (TRIM59-IFT80)
NM_020800.3:c.1381-61_1381-60insCT (IFT80) MANE Select	NP_065851.1:n.1381-61_1381-60insCT
NM_001190241.2:c.970-61_970-60insCT (IFT80)	NP_001177170.1:n.970-61_970-60insCT
NM_001190242.2:c.970-61_970-60insCT (IFT80)	NP_001177171.1:n.970-61_970-60insCT