Canonical Allele Identifier: CA2147731382

Gene: IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985792G= , CM000676.2:g.75985792G=	GRCh38
NC_000014.8:g.76452135G= , CM000676.1:g.76452135G=	GRCh37
NC_000014.7:g.75521888G=	NCBI36
NG_011715.1:g.958C= , LRG_399:g.958C=
NG_031957.1:g.5040G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.6G= MANE Select	ENSP00000324177.6:p.Glu2=
ENST00000679083.1:c.-241G=	ENSP00000504736.1:n.-241G=
ENST00000238628.10:c.6G=	ENSP00000238628.6:p.Glu2=
ENST00000314067.10:c.6G=	ENSP00000324177.6:p.Glu2=
ENST00000542766.5:c.6G=	ENSP00000440064.1:p.Glu2=
ENST00000554026.5:n.13G=
ENST00000555305.5:n.13G=
ENST00000555370.5:c.6G=	ENSP00000452051.1:p.Glu2=
ENST00000555677.5:n.90-3093G=
ENST00000556742.1:c.6G=	ENSP00000451096.1:p.Glu2=
NM_001102564.1:c.6G=	NP_001096034.1:p.Glu2=
NM_001255995.1:c.6G=	NP_001242924.1:p.Glu2=
NM_052873.2:c.6G=	NP_443105.2:p.Glu2=
NR_045664.1:n.40G=
NR_045665.1:n.40G=
NM_001102564.2:c.6G=	NP_001096034.1:p.Glu2=
NM_001255995.2:c.6G=	NP_001242924.1:p.Glu2=
NM_052873.3:c.6G=	NP_443105.2:p.Glu2=
NM_001102564.3:c.6G= MANE Select	NP_001096034.1:p.Glu2=
NM_001255995.3:c.6G=	NP_001242924.1:p.Glu2=
NR_045664.2:n.30G=
NR_045665.2:n.30G=