Canonical Allele Identifier: CA2147731386

Gene: IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985796T= , CM000676.2:g.75985796T=	GRCh38
NC_000014.8:g.76452139T= , CM000676.1:g.76452139T=	GRCh37
NC_000014.7:g.75521892T=	NCBI36
NG_011715.1:g.954A= , LRG_399:g.954A=
NG_031957.1:g.5044T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.10T= MANE Select	ENSP00000324177.6:p.Leu4=
ENST00000679083.1:c.-237T=	ENSP00000504736.1:n.-237T=
ENST00000238628.10:c.10T=	ENSP00000238628.6:p.Leu4=
ENST00000314067.10:c.10T=	ENSP00000324177.6:p.Leu4=
ENST00000542766.5:c.10T=	ENSP00000440064.1:p.Leu4=
ENST00000553338.1:n.3T=
ENST00000554026.5:n.17T=
ENST00000555305.5:n.17T=
ENST00000555370.5:c.10T=	ENSP00000452051.1:p.Leu4=
ENST00000555677.5:n.90-3089T=
ENST00000556742.1:c.10T=	ENSP00000451096.1:p.Leu4=
NM_001102564.1:c.10T=	NP_001096034.1:p.Leu4=
NM_001255995.1:c.10T=	NP_001242924.1:p.Leu4=
NM_052873.2:c.10T=	NP_443105.2:p.Leu4=
NR_045664.1:n.44T=
NR_045665.1:n.44T=
NM_001102564.2:c.10T=	NP_001096034.1:p.Leu4=
NM_001255995.2:c.10T=	NP_001242924.1:p.Leu4=
NM_052873.3:c.10T=	NP_443105.2:p.Leu4=
NM_001102564.3:c.10T= MANE Select	NP_001096034.1:p.Leu4=
NM_001255995.3:c.10T=	NP_001242924.1:p.Leu4=
NR_045664.2:n.34T=
NR_045665.2:n.34T=