Canonical Allele Identifier: CA7280565

Gene: IFT43

Linked Data

• dbSNP Id: rs769724508
• ExAC: 14:76452131 T / C
• gnomAD v2: 14-76452131-T-C
• gnomAD v4: 14-75985788-T-C
• MyVariant Identifiers: chr14:g.76452131T>C (hg19) ; chr14:g.75985788T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985788T>C , CM000676.2:g.75985788T>C	GRCh38
NC_000014.8:g.76452131T>C , CM000676.1:g.76452131T>C	GRCh37
NC_000014.7:g.75521884T>C	NCBI36
NG_011715.1:g.962A>G , LRG_399:g.962A>G
NG_031957.1:g.5036T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.2T>C MANE Select	ENSP00000324177.6:p.Met1Thr
ENST00000679083.1:c.-245T>C	ENSP00000504736.1:n.-245T>C
ENST00000238628.10:c.2T>C	ENSP00000238628.6:p.Met1Thr
ENST00000314067.10:c.2T>C	ENSP00000324177.6:p.Met1Thr
ENST00000542766.5:c.2T>C	ENSP00000440064.1:p.Met1Thr
ENST00000554026.5:n.9T>C
ENST00000555305.5:n.9T>C
ENST00000555370.5:c.2T>C	ENSP00000452051.1:p.Met1Thr
ENST00000555677.5:n.90-3097T>C
ENST00000556742.1:c.2T>C	ENSP00000451096.1:p.Met1Thr
NM_001102564.1:c.2T>C	NP_001096034.1:p.Met1Thr
NM_001255995.1:c.2T>C	NP_001242924.1:p.Met1Thr
NM_052873.2:c.2T>C	NP_443105.2:p.Met1Thr
NR_045664.1:n.36T>C
NR_045665.1:n.36T>C
NM_001102564.2:c.2T>C	NP_001096034.1:p.Met1Thr
NM_001255995.2:c.2T>C	NP_001242924.1:p.Met1Thr
NM_052873.3:c.2T>C	NP_443105.2:p.Met1Thr
NM_001102564.3:c.2T>C MANE Select	NP_001096034.1:p.Met1Thr
NM_001255995.3:c.2T>C	NP_001242924.1:p.Met1Thr
NR_045664.2:n.26T>C
NR_045665.2:n.26T>C