Canonical Allele Identifier: CA390472790

Gene: IFT43

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985789G>A , CM000676.2:g.75985789G>A	GRCh38
NC_000014.8:g.76452132G>A , CM000676.1:g.76452132G>A	GRCh37
NC_000014.7:g.75521885G>A	NCBI36
NG_011715.1:g.961C>T , LRG_399:g.961C>T
NG_031957.1:g.5037G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.3G>A MANE Select	ENSP00000324177.6:p.Met1Ile
ENST00000679083.1:c.-244G>A	ENSP00000504736.1:n.-244G>A
ENST00000238628.10:c.3G>A	ENSP00000238628.6:p.Met1Ile
ENST00000314067.10:c.3G>A	ENSP00000324177.6:p.Met1Ile
ENST00000542766.5:c.3G>A	ENSP00000440064.1:p.Met1Ile
ENST00000554026.5:n.10G>A
ENST00000555305.5:n.10G>A
ENST00000555370.5:c.3G>A	ENSP00000452051.1:p.Met1Ile
ENST00000555677.5:n.90-3096G>A
ENST00000556742.1:c.3G>A	ENSP00000451096.1:p.Met1Ile
NM_001102564.1:c.3G>A	NP_001096034.1:p.Met1Ile
NM_001255995.1:c.3G>A	NP_001242924.1:p.Met1Ile
NM_052873.2:c.3G>A	NP_443105.2:p.Met1Ile
NR_045664.1:n.37G>A
NR_045665.1:n.37G>A
NM_001102564.2:c.3G>A	NP_001096034.1:p.Met1Ile
NM_001255995.2:c.3G>A	NP_001242924.1:p.Met1Ile
NM_052873.3:c.3G>A	NP_443105.2:p.Met1Ile
NM_001102564.3:c.3G>A MANE Select	NP_001096034.1:p.Met1Ile
NM_001255995.3:c.3G>A	NP_001242924.1:p.Met1Ile
NR_045664.2:n.27G>A
NR_045665.2:n.27G>A