Canonical Allele Identifier: CA1415171896

Gene: IFT80 TRIM59-IFT80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160377485G= , CM000665.2:g.160377485G=	GRCh38
NC_000003.11:g.160095273G= , CM000665.1:g.160095273G=	GRCh37
NC_000003.10:g.161577967G=	NCBI36
NG_022932.1:g.27048C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020800.3:c.315C= (IFT80) MANE Select	NP_065851.1:p.His105=
ENST00000326448.12:c.315C= (IFT80) MANE Select	ENSP00000312778.7:p.His105=
NM_001190241.1:c.-97C= (IFT80)	NP_001177170.1:n.-97C=
NM_001190241.2:c.-97C= (IFT80)	NP_001177170.1:n.-97C=
NM_001190242.1:c.-97C= (IFT80)	NP_001177171.1:n.-97C=
NM_001190242.2:c.-97C= (IFT80)	NP_001177171.1:n.-97C=
NM_020800.2:c.315C= (IFT80)	NP_065851.1:p.His105=
NR_148401.1:n.1148-11333C= (TRIM59-IFT80)
NR_148402.1:n.2559C= (TRIM59-IFT80)
NR_148403.1:n.2826C= (TRIM59-IFT80)
ENST00000326448.11:c.315C= (IFT80)	ENSP00000312778.7:p.His105=
ENST00000465537.5:c.-97C= (IFT80)	ENSP00000418602.1:n.-97C=
ENST00000465972.5:n.520C= (IFT80)
ENST00000468218.5:c.-97C= (IFT80)	ENSP00000417057.1:n.-97C=
ENST00000468327.1:n.531C= (IFT80)
ENST00000472773.5:n.439C= (IFT80)
ENST00000475677.5:c.-97C= (IFT80)	ENSP00000419458.1:n.-97C=
ENST00000477495.5:n.461C= (IFT80)
ENST00000478370.5:c.-97C= (IFT80)	ENSP00000420758.1:n.-97C=
ENST00000478460.5:n.132C= (IFT80)
ENST00000482317.5:c.*52C= (IFT80)	ENSP00000418497.1:n.*52C=
ENST00000483465.5:c.-97C= (IFT80)	ENSP00000418196.1:n.-97C=
ENST00000483754.1:c.953-11333C= (TRIM59-IFT80)	ENSP00000456272.1:n.953-11333C=
ENST00000486856.5:c.-97C= (IFT80)	ENSP00000417861.1:n.-97C=
ENST00000487943.5:n.1644C= (IFT80)
ENST00000489004.5:c.315C= (IFT80)	ENSP00000418455.1:p.His105=
ENST00000496589.5:c.-97C= (IFT80)	ENSP00000420646.1:n.-97C=
ENST00000498409.5:c.315C= (IFT80)	ENSP00000420001.1:p.His105=