Canonical Allele Identifier: CA355192039

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• MyVariant Identifiers: chr3:g.160000293C>T (hg19) ; chr3:g.160282505C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282505C>T , CM000665.2:g.160282505C>T	GRCh38
NC_000003.11:g.160000293C>T , CM000665.1:g.160000293C>T	GRCh37
NC_000003.10:g.161482987C>T	NCBI36
NG_022932.1:g.122028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1489G>A (IFT80) MANE Select	ENSP00000312778.7:p.Gly497Arg
ENST00000326448.11:c.1489G>A (IFT80)	ENSP00000312778.7:p.Gly497Arg
ENST00000483465.5:c.1078G>A (IFT80)	ENSP00000418196.1:p.Gly360Arg
ENST00000483754.1:c.2002G>A (TRIM59-IFT80)	ENSP00000456272.1:p.Gly668Arg
ENST00000487943.5:n.2708G>A (IFT80)
ENST00000496589.5:c.1078G>A (IFT80)	ENSP00000420646.1:p.Gly360Arg
NM_001190241.1:c.1078G>A (IFT80)	NP_001177170.1:p.Gly360Arg
NM_001190242.1:c.1078G>A (IFT80)	NP_001177171.1:p.Gly360Arg
NM_020800.2:c.1489G>A (IFT80)	NP_065851.1:p.Gly497Arg
XR_924138.1:n.2900-7167C>T (C3orf80)
NR_148401.1:n.2197G>A (TRIM59-IFT80)
NR_148402.1:n.3733G>A (TRIM59-IFT80)
NR_148403.1:n.4000G>A (TRIM59-IFT80)
NM_020800.3:c.1489G>A (IFT80) MANE Select	NP_065851.1:p.Gly497Arg
NM_001190241.2:c.1078G>A (IFT80)	NP_001177170.1:p.Gly360Arg
NM_001190242.2:c.1078G>A (IFT80)	NP_001177171.1:p.Gly360Arg