Canonical Allele Identifier: CA1415115390

Gene: IFT80 TRIM59-IFT80 C3orf80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282582T= , CM000665.2:g.160282582T=	GRCh38
NC_000003.11:g.160000370T= , CM000665.1:g.160000370T=	GRCh37
NC_000003.10:g.161483064T=	NCBI36
NG_022932.1:g.121951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1412A= (IFT80) MANE Select	ENSP00000312778.7:p.Lys471=
ENST00000326448.11:c.1412A= (IFT80)	ENSP00000312778.7:p.Lys471=
ENST00000483465.5:c.1001A= (IFT80)	ENSP00000418196.1:p.Lys334=
ENST00000483754.1:c.1925A= (TRIM59-IFT80)	ENSP00000456272.1:p.Lys642=
ENST00000487943.5:n.2631A= (IFT80)
ENST00000496589.5:c.1001A= (IFT80)	ENSP00000420646.1:p.Lys334=
NM_001190241.1:c.1001A= (IFT80)	NP_001177170.1:p.Lys334=
NM_001190242.1:c.1001A= (IFT80)	NP_001177171.1:p.Lys334=
NM_020800.2:c.1412A= (IFT80)	NP_065851.1:p.Lys471=
XR_924138.1:n.2900-7090T= (C3orf80)
NR_148401.1:n.2120A= (TRIM59-IFT80)
NR_148402.1:n.3656A= (TRIM59-IFT80)
NR_148403.1:n.3923A= (TRIM59-IFT80)
NM_020800.3:c.1412A= (IFT80) MANE Select	NP_065851.1:p.Lys471=
NM_001190241.2:c.1001A= (IFT80)	NP_001177170.1:p.Lys334=
NM_001190242.2:c.1001A= (IFT80)	NP_001177171.1:p.Lys334=