Canonical Allele Identifier: CA355191969

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• MyVariant Identifiers: chr3:g.160000278T>G (hg19) ; chr3:g.160282490T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282490T>G , CM000665.2:g.160282490T>G	GRCh38
NC_000003.11:g.160000278T>G , CM000665.1:g.160000278T>G	GRCh37
NC_000003.10:g.161482972T>G	NCBI36
NG_022932.1:g.122043A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326448.12:c.1504A>C (IFT80) MANE Select	ENSP00000312778.7:p.Ile502Leu
ENST00000326448.11:c.1504A>C (IFT80)	ENSP00000312778.7:p.Ile502Leu
ENST00000483465.5:c.1093A>C (IFT80)	ENSP00000418196.1:p.Ile365Leu
ENST00000483754.1:c.2017A>C (TRIM59-IFT80)	ENSP00000456272.1:p.Ile673Leu
ENST00000487943.5:n.2723A>C (IFT80)
ENST00000496589.5:c.1093A>C (IFT80)	ENSP00000420646.1:p.Ile365Leu
NM_001190241.1:c.1093A>C (IFT80)	NP_001177170.1:p.Ile365Leu
NM_001190242.1:c.1093A>C (IFT80)	NP_001177171.1:p.Ile365Leu
NM_020800.2:c.1504A>C (IFT80)	NP_065851.1:p.Ile502Leu
XR_924138.1:n.2900-7182T>G (C3orf80)
NR_148401.1:n.2212A>C (TRIM59-IFT80)
NR_148402.1:n.3748A>C (TRIM59-IFT80)
NR_148403.1:n.4015A>C (TRIM59-IFT80)
NM_020800.3:c.1504A>C (IFT80) MANE Select	NP_065851.1:p.Ile502Leu
NM_001190241.2:c.1093A>C (IFT80)	NP_001177170.1:p.Ile365Leu
NM_001190242.2:c.1093A>C (IFT80)	NP_001177171.1:p.Ile365Leu