Canonical Allele Identifier: CA2996915445
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985797dup , CM000676.2:g.75985797dup GRCh38
NC_000014.8:g.76452140dup , CM000676.1:g.76452140dup GRCh37
NC_000014.7:g.75521893dup NCBI36
NG_011715.1:g.955dup , LRG_399:g.955dup
NG_031957.1:g.5045dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000314067.11:c.11dup MANE Select ENSP00000324177.6:p.Leu4PhefsTer?
ENST00000679083.1:c.-236dup ENSP00000504736.1:n.-236dup
ENST00000238628.10:c.11dup ENSP00000238628.6:p.Leu4PhefsTer?
ENST00000314067.10:c.11dup ENSP00000324177.6:p.Leu4PhefsTer?
ENST00000542766.5:c.11dup ENSP00000440064.1:p.Leu4PhefsTer?
ENST00000553338.1:n.4dup
ENST00000554026.5:n.18dup
ENST00000555305.5:n.18dup
ENST00000555370.5:c.11dup ENSP00000452051.1:p.Leu4PhefsTer?
ENST00000555677.5:n.90-3088dup
ENST00000556742.1:c.11dup ENSP00000451096.1:p.Leu4PhefsTer?
NM_001102564.1:c.11dup NP_001096034.1:p.Leu4PhefsTer?
NM_001255995.1:c.11dup NP_001242924.1:p.Leu4PhefsTer?
NM_052873.2:c.11dup NP_443105.2:p.Leu4PhefsTer?
NR_045664.1:n.45dup
NR_045665.1:n.45dup
NM_001102564.2:c.11dup NP_001096034.1:p.Leu4PhefsTer?
NM_001255995.2:c.11dup NP_001242924.1:p.Leu4PhefsTer?
NM_052873.3:c.11dup NP_443105.2:p.Leu4PhefsTer?
NM_001102564.3:c.11dup MANE Select NP_001096034.1:p.Leu4PhefsTer?
NM_001255995.3:c.11dup NP_001242924.1:p.Leu4PhefsTer?
NR_045664.2:n.35dup
NR_045665.2:n.35dup