Canonical Allele Identifier: CA2950881796
Gene: IFT43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75985696dup , CM000676.2:g.75985696dup GRCh38
NC_000014.8:g.76452039dup , CM000676.1:g.76452039dup GRCh37
NC_000014.7:g.75521792dup NCBI36
NG_011715.1:g.1056dup , LRG_399:g.1056dup
NG_031957.1:g.4944dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000555677.5:n.90-3189dup