Canonical Allele Identifier: CA390472809

Gene: IFT43

Linked Data

• MyVariant Identifiers: chr14:g.76452140T>G (hg19) ; chr14:g.75985797T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985797T>G , CM000676.2:g.75985797T>G	GRCh38
NC_000014.8:g.76452140T>G , CM000676.1:g.76452140T>G	GRCh37
NC_000014.7:g.75521893T>G	NCBI36
NG_011715.1:g.953A>C , LRG_399:g.953A>C
NG_031957.1:g.5045T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.11T>G MANE Select	ENSP00000324177.6:p.Leu4Trp
ENST00000679083.1:c.-236T>G	ENSP00000504736.1:n.-236T>G
ENST00000238628.10:c.11T>G	ENSP00000238628.6:p.Leu4Trp
ENST00000314067.10:c.11T>G	ENSP00000324177.6:p.Leu4Trp
ENST00000542766.5:c.11T>G	ENSP00000440064.1:p.Leu4Trp
ENST00000553338.1:n.4T>G
ENST00000554026.5:n.18T>G
ENST00000555305.5:n.18T>G
ENST00000555370.5:c.11T>G	ENSP00000452051.1:p.Leu4Trp
ENST00000555677.5:n.90-3088T>G
ENST00000556742.1:c.11T>G	ENSP00000451096.1:p.Leu4Trp
NM_001102564.1:c.11T>G	NP_001096034.1:p.Leu4Trp
NM_001255995.1:c.11T>G	NP_001242924.1:p.Leu4Trp
NM_052873.2:c.11T>G	NP_443105.2:p.Leu4Trp
NR_045664.1:n.45T>G
NR_045665.1:n.45T>G
NM_001102564.2:c.11T>G	NP_001096034.1:p.Leu4Trp
NM_001255995.2:c.11T>G	NP_001242924.1:p.Leu4Trp
NM_052873.3:c.11T>G	NP_443105.2:p.Leu4Trp
NM_001102564.3:c.11T>G MANE Select	NP_001096034.1:p.Leu4Trp
NM_001255995.3:c.11T>G	NP_001242924.1:p.Leu4Trp
NR_045664.2:n.35T>G
NR_045665.2:n.35T>G