Canonical Allele Identifier: CA2147731385

Gene: IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985795T= , CM000676.2:g.75985795T=	GRCh38
NC_000014.8:g.76452138T= , CM000676.1:g.76452138T=	GRCh37
NC_000014.7:g.75521891T=	NCBI36
NG_011715.1:g.955A= , LRG_399:g.955A=
NG_031957.1:g.5043T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.9T= MANE Select	ENSP00000324177.6:p.Asp3=
ENST00000679083.1:c.-238T=	ENSP00000504736.1:n.-238T=
ENST00000238628.10:c.9T=	ENSP00000238628.6:p.Asp3=
ENST00000314067.10:c.9T=	ENSP00000324177.6:p.Asp3=
ENST00000542766.5:c.9T=	ENSP00000440064.1:p.Asp3=
ENST00000553338.1:n.2T=
ENST00000554026.5:n.16T=
ENST00000555305.5:n.16T=
ENST00000555370.5:c.9T=	ENSP00000452051.1:p.Asp3=
ENST00000555677.5:n.90-3090T=
ENST00000556742.1:c.9T=	ENSP00000451096.1:p.Asp3=
NM_001102564.1:c.9T=	NP_001096034.1:p.Asp3=
NM_001255995.1:c.9T=	NP_001242924.1:p.Asp3=
NM_052873.2:c.9T=	NP_443105.2:p.Asp3=
NR_045664.1:n.43T=
NR_045665.1:n.43T=
NM_001102564.2:c.9T=	NP_001096034.1:p.Asp3=
NM_001255995.2:c.9T=	NP_001242924.1:p.Asp3=
NM_052873.3:c.9T=	NP_443105.2:p.Asp3=
NM_001102564.3:c.9T= MANE Select	NP_001096034.1:p.Asp3=
NM_001255995.3:c.9T=	NP_001242924.1:p.Asp3=
NR_045664.2:n.33T=
NR_045665.2:n.33T=