Canonical Allele Identifier: CA2668375867

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• gnomAD v4: 3-160282500-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282502del , CM000665.2:g.160282502del	GRCh38
NC_000003.11:g.160000290del , CM000665.1:g.160000290del	GRCh37
NC_000003.10:g.161482984del	NCBI36
NG_022932.1:g.122032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1493del (IFT80) MANE Select	ENSP00000312778.7:p.Lys498ArgfsTer?
ENST00000326448.11:c.1493del (IFT80)	ENSP00000312778.7:p.Lys498ArgfsTer?
ENST00000483465.5:c.1082del (IFT80)	ENSP00000418196.1:p.Lys361ArgfsTer?
ENST00000483754.1:c.2006del (TRIM59-IFT80)	ENSP00000456272.1:p.Lys669ArgfsTer?
ENST00000487943.5:n.2712del (IFT80)
ENST00000496589.5:c.1082del (IFT80)	ENSP00000420646.1:p.Lys361ArgfsTer?
NM_001190241.1:c.1082del (IFT80)	NP_001177170.1:p.Lys361ArgfsTer?
NM_001190242.1:c.1082del (IFT80)	NP_001177171.1:p.Lys361ArgfsTer?
NM_020800.2:c.1493del (IFT80)	NP_065851.1:p.Lys498ArgfsTer?
XR_924138.1:n.2900-7170del (C3orf80)
NR_148401.1:n.2201del (TRIM59-IFT80)
NR_148402.1:n.3737del (TRIM59-IFT80)
NR_148403.1:n.4004del (TRIM59-IFT80)
NM_020800.3:c.1493del (IFT80) MANE Select	NP_065851.1:p.Lys498ArgfsTer?
NM_001190241.2:c.1082del (IFT80)	NP_001177170.1:p.Lys361ArgfsTer?
NM_001190242.2:c.1082del (IFT80)	NP_001177171.1:p.Lys361ArgfsTer?