Canonical Allele Identifier: CA390472808

Gene: IFT43

Linked Data - Variant Effect Evidence

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.11T>C MANE Select	ENSP00000324177.6:p.Leu4Ser
ENST00000679083.1:c.-236T>C	ENSP00000504736.1:n.-236T>C
ENST00000238628.10:c.11T>C	ENSP00000238628.6:p.Leu4Ser
ENST00000314067.10:c.11T>C	ENSP00000324177.6:p.Leu4Ser
ENST00000542766.5:c.11T>C	ENSP00000440064.1:p.Leu4Ser
ENST00000553338.1:n.4T>C
ENST00000554026.5:n.18T>C
ENST00000555305.5:n.18T>C
ENST00000555370.5:c.11T>C	ENSP00000452051.1:p.Leu4Ser
ENST00000555677.5:n.90-3088T>C
ENST00000556742.1:c.11T>C	ENSP00000451096.1:p.Leu4Ser
NM_001102564.1:c.11T>C	NP_001096034.1:p.Leu4Ser
NM_001255995.1:c.11T>C	NP_001242924.1:p.Leu4Ser
NM_052873.2:c.11T>C	NP_443105.2:p.Leu4Ser
NR_045664.1:n.45T>C
NR_045665.1:n.45T>C
NM_001102564.2:c.11T>C	NP_001096034.1:p.Leu4Ser
NM_001255995.2:c.11T>C	NP_001242924.1:p.Leu4Ser
NM_052873.3:c.11T>C	NP_443105.2:p.Leu4Ser
NM_001102564.3:c.11T>C MANE Select	NP_001096034.1:p.Leu4Ser
NM_001255995.3:c.11T>C	NP_001242924.1:p.Leu4Ser
NR_045664.2:n.35T>C
NR_045665.2:n.35T>C