Canonical Allele Identifier: CA1415115659

Gene: IFT80 TRIM59-IFT80 C3orf80

Linked Data

• dbSNP Id: rs1714793702
• gnomAD v3: 3-160282841-TA-T
• gnomAD v4: 3-160282841-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160282842del , CM000665.2:g.160282842del	GRCh38
NC_000003.11:g.160000630del , CM000665.1:g.160000630del	GRCh37
NC_000003.10:g.161483324del	NCBI36
NG_022932.1:g.121691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326448.12:c.1381-229del (IFT80) MANE Select	ENSP00000312778.7:n.1381-229del
ENST00000326448.11:c.1381-229del (IFT80)	ENSP00000312778.7:n.1381-229del
ENST00000483465.5:c.970-229del (IFT80)	ENSP00000418196.1:n.970-229del
ENST00000483754.1:c.1894-229del (TRIM59-IFT80)	ENSP00000456272.1:n.1894-229del
ENST00000487943.5:n.2600-229del (IFT80)
ENST00000496589.5:c.970-229del (IFT80)	ENSP00000420646.1:n.970-229del
NM_001190241.1:c.970-229del (IFT80)	NP_001177170.1:n.970-229del
NM_001190242.1:c.970-229del (IFT80)	NP_001177171.1:n.970-229del
NM_020800.2:c.1381-229del (IFT80)	NP_065851.1:n.1381-229del
XR_924138.1:n.2900-6830del (C3orf80)
NR_148401.1:n.2089-229del (TRIM59-IFT80)
NR_148402.1:n.3625-229del (TRIM59-IFT80)
NR_148403.1:n.3892-229del (TRIM59-IFT80)
NM_020800.3:c.1381-229del (IFT80) MANE Select	NP_065851.1:n.1381-229del
NM_001190241.2:c.970-229del (IFT80)	NP_001177170.1:n.970-229del
NM_001190242.2:c.970-229del (IFT80)	NP_001177171.1:n.970-229del