Canonical Allele Identifier: CA2759121208

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282636_160282638del , CM000665.2:g.160282636_160282638del	GRCh38
NC_000003.11:g.160000424_160000426del , CM000665.1:g.160000424_160000426del	GRCh37
NC_000003.10:g.161483118_161483120del	NCBI36
NG_022932.1:g.121896_121898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-24_1381-22del (IFT80) MANE Select	ENSP00000312778.7:n.1381-24_1381-22del
ENST00000326448.11:c.1381-24_1381-22del (IFT80)	ENSP00000312778.7:n.1381-24_1381-22del
ENST00000483465.5:c.970-24_970-22del (IFT80)	ENSP00000418196.1:n.970-24_970-22del
ENST00000483754.1:c.1894-24_1894-22del (TRIM59-IFT80)	ENSP00000456272.1:n.1894-24_1894-22del
ENST00000487943.5:n.2600-24_2600-22del (IFT80)
ENST00000496589.5:c.970-24_970-22del (IFT80)	ENSP00000420646.1:n.970-24_970-22del
NM_001190241.1:c.970-24_970-22del (IFT80)	NP_001177170.1:n.970-24_970-22del
NM_001190242.1:c.970-24_970-22del (IFT80)	NP_001177171.1:n.970-24_970-22del
NM_020800.2:c.1381-24_1381-22del (IFT80)	NP_065851.1:n.1381-24_1381-22del
XR_924138.1:n.2900-7036_2900-7034del (C3orf80)
NR_148401.1:n.2089-24_2089-22del (TRIM59-IFT80)
NR_148402.1:n.3625-24_3625-22del (TRIM59-IFT80)
NR_148403.1:n.3892-24_3892-22del (TRIM59-IFT80)
NM_020800.3:c.1381-24_1381-22del (IFT80) MANE Select	NP_065851.1:n.1381-24_1381-22del
NM_001190241.2:c.970-24_970-22del (IFT80)	NP_001177170.1:n.970-24_970-22del
NM_001190242.2:c.970-24_970-22del (IFT80)	NP_001177171.1:n.970-24_970-22del