Canonical Allele Identifier: CA436487957

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• MyVariant Identifiers: chr3:g.160000393G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282605G>A , CM000665.2:g.160282605G>A	GRCh38
NC_000003.11:g.160000393G>A , CM000665.1:g.160000393G>A	GRCh37
NC_000003.10:g.161483087G>A	NCBI36
NG_022932.1:g.121928C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1389C>T (IFT80) MANE Select	ENSP00000312778.7:p.Ile463=
ENST00000326448.11:c.1389C>T (IFT80)	ENSP00000312778.7:p.Ile463=
ENST00000483465.5:c.978C>T (IFT80)	ENSP00000418196.1:p.Ile326=
ENST00000483754.1:c.1902C>T (TRIM59-IFT80)	ENSP00000456272.1:p.Ile634=
ENST00000487943.5:n.2608C>T (IFT80)
ENST00000496589.5:c.978C>T (IFT80)	ENSP00000420646.1:p.Ile326=
NM_001190241.1:c.978C>T (IFT80)	NP_001177170.1:p.Ile326=
NM_001190242.1:c.978C>T (IFT80)	NP_001177171.1:p.Ile326=
NM_020800.2:c.1389C>T (IFT80)	NP_065851.1:p.Ile463=
XR_924138.1:n.2900-7067G>A (C3orf80)
NR_148401.1:n.2097C>T (TRIM59-IFT80)
NR_148402.1:n.3633C>T (TRIM59-IFT80)
NR_148403.1:n.3900C>T (TRIM59-IFT80)
NM_020800.3:c.1389C>T (IFT80) MANE Select	NP_065851.1:p.Ile463=
NM_001190241.2:c.978C>T (IFT80)	NP_001177170.1:p.Ile326=
NM_001190242.2:c.978C>T (IFT80)	NP_001177171.1:p.Ile326=