Canonical Allele Identifier: CA2759121249

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282681_160282682del , CM000665.2:g.160282681_160282682del	GRCh38
NC_000003.11:g.160000469_160000470del , CM000665.1:g.160000469_160000470del	GRCh37
NC_000003.10:g.161483163_161483164del	NCBI36
NG_022932.1:g.121851_121852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-69_1381-68del (IFT80) MANE Select	ENSP00000312778.7:n.1381-69_1381-68del
ENST00000326448.11:c.1381-69_1381-68del (IFT80)	ENSP00000312778.7:n.1381-69_1381-68del
ENST00000483465.5:c.970-69_970-68del (IFT80)	ENSP00000418196.1:n.970-69_970-68del
ENST00000483754.1:c.1894-69_1894-68del (TRIM59-IFT80)	ENSP00000456272.1:n.1894-69_1894-68del
ENST00000487943.5:n.2600-69_2600-68del (IFT80)
ENST00000496589.5:c.970-69_970-68del (IFT80)	ENSP00000420646.1:n.970-69_970-68del
NM_001190241.1:c.970-69_970-68del (IFT80)	NP_001177170.1:n.970-69_970-68del
NM_001190242.1:c.970-69_970-68del (IFT80)	NP_001177171.1:n.970-69_970-68del
NM_020800.2:c.1381-69_1381-68del (IFT80)	NP_065851.1:n.1381-69_1381-68del
XR_924138.1:n.2900-6991_2900-6990del (C3orf80)
NR_148401.1:n.2089-69_2089-68del (TRIM59-IFT80)
NR_148402.1:n.3625-69_3625-68del (TRIM59-IFT80)
NR_148403.1:n.3892-69_3892-68del (TRIM59-IFT80)
NM_020800.3:c.1381-69_1381-68del (IFT80) MANE Select	NP_065851.1:n.1381-69_1381-68del
NM_001190241.2:c.970-69_970-68del (IFT80)	NP_001177170.1:n.970-69_970-68del
NM_001190242.2:c.970-69_970-68del (IFT80)	NP_001177171.1:n.970-69_970-68del