Canonical Allele Identifier: CA1415140905

Gene: IFT80 TRIM59-IFT80

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.160356069C= , CM000665.2:g.160356069C=	GRCh38
NC_000003.11:g.160073857C= , CM000665.1:g.160073857C=	GRCh37
NC_000003.10:g.161556551C=	NCBI36
NG_022932.1:g.48464G=

Transcript Alleles

HGVS	Amino-acid Change
NM_020800.3:c.721G= (IFT80) MANE Select	NP_065851.1:p.Gly241=
ENST00000326448.12:c.721G= (IFT80) MANE Select	ENSP00000312778.7:p.Gly241=
NM_001190241.1:c.310G= (IFT80)	NP_001177170.1:p.Gly104=
NM_001190241.2:c.310G= (IFT80)	NP_001177170.1:p.Gly104=
NM_001190242.1:c.310G= (IFT80)	NP_001177171.1:p.Gly104=
NM_001190242.2:c.310G= (IFT80)	NP_001177171.1:p.Gly104=
NM_020800.2:c.721G= (IFT80)	NP_065851.1:p.Gly241=
NR_148401.1:n.1429G= (TRIM59-IFT80)
NR_148402.1:n.2965G= (TRIM59-IFT80)
NR_148403.1:n.3232G= (TRIM59-IFT80)
ENST00000326448.11:c.721G= (IFT80)	ENSP00000312778.7:p.Gly241=
ENST00000465537.5:c.310G= (IFT80)	ENSP00000418602.1:p.Gly104=
ENST00000472555.5:c.93G= (IFT80)
ENST00000478460.5:n.428G= (IFT80)
ENST00000483465.5:c.310G= (IFT80)	ENSP00000418196.1:p.Gly104=
ENST00000483754.1:c.1234G= (TRIM59-IFT80)	ENSP00000456272.1:p.Gly412=
ENST00000484963.5:c.326G= (IFT80)	ENSP00000420260.1:n.326G=
ENST00000487943.5:n.1940G= (IFT80)
ENST00000496589.5:c.310G= (IFT80)	ENSP00000420646.1:p.Gly104=