Canonical Allele Identifier: CA2147731388

Gene: IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985799C= , CM000676.2:g.75985799C=	GRCh38
NC_000014.8:g.76452142C= , CM000676.1:g.76452142C=	GRCh37
NC_000014.7:g.75521895C=	NCBI36
NG_011715.1:g.951G= , LRG_399:g.951G=
NG_031957.1:g.5047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.13C= MANE Select	ENSP00000324177.6:p.Leu5=
ENST00000679083.1:c.-234C=	ENSP00000504736.1:n.-234C=
ENST00000238628.10:c.13C=	ENSP00000238628.6:p.Leu5=
ENST00000314067.10:c.13C=	ENSP00000324177.6:p.Leu5=
ENST00000542766.5:c.13C=	ENSP00000440064.1:p.Leu5=
ENST00000553338.1:n.6C=
ENST00000554026.5:n.20C=
ENST00000555305.5:n.20C=
ENST00000555370.5:c.13C=	ENSP00000452051.1:p.Leu5=
ENST00000555677.5:n.90-3086C=
ENST00000556742.1:c.13C=	ENSP00000451096.1:p.Leu5=
NM_001102564.1:c.13C=	NP_001096034.1:p.Leu5=
NM_001255995.1:c.13C=	NP_001242924.1:p.Leu5=
NM_052873.2:c.13C=	NP_443105.2:p.Leu5=
NR_045664.1:n.47C=
NR_045665.1:n.47C=
NM_001102564.2:c.13C=	NP_001096034.1:p.Leu5=
NM_001255995.2:c.13C=	NP_001242924.1:p.Leu5=
NM_052873.3:c.13C=	NP_443105.2:p.Leu5=
NM_001102564.3:c.13C= MANE Select	NP_001096034.1:p.Leu5=
NM_001255995.3:c.13C=	NP_001242924.1:p.Leu5=
NR_045664.2:n.37C=
NR_045665.2:n.37C=