Canonical Allele Identifier: CA2147731378

Gene: IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75985787A= , CM000676.2:g.75985787A=	GRCh38
NC_000014.8:g.76452130A= , CM000676.1:g.76452130A=	GRCh37
NC_000014.7:g.75521883A=	NCBI36
NG_011715.1:g.963T= , LRG_399:g.963T=
NG_031957.1:g.5035A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314067.11:c.1A= MANE Select	ENSP00000324177.6:p.Met1=
ENST00000679083.1:c.-246A=	ENSP00000504736.1:n.-246A=
ENST00000238628.10:c.1A=	ENSP00000238628.6:p.Met1=
ENST00000314067.10:c.1A=	ENSP00000324177.6:p.Met1=
ENST00000542766.5:c.1A=	ENSP00000440064.1:p.Met1=
ENST00000554026.5:n.8A=
ENST00000555305.5:n.8A=
ENST00000555370.5:c.1A=	ENSP00000452051.1:p.Met1=
ENST00000555677.5:n.90-3098A=
ENST00000556742.1:c.1A=	ENSP00000451096.1:p.Met1=
NM_001102564.1:c.1A=	NP_001096034.1:p.Met1=
NM_001255995.1:c.1A=	NP_001242924.1:p.Met1=
NM_052873.2:c.1A=	NP_443105.2:p.Met1=
NR_045664.1:n.35A=
NR_045665.1:n.35A=
NM_001102564.2:c.1A=	NP_001096034.1:p.Met1=
NM_001255995.2:c.1A=	NP_001242924.1:p.Met1=
NM_052873.3:c.1A=	NP_443105.2:p.Met1=
NM_001102564.3:c.1A= MANE Select	NP_001096034.1:p.Met1=
NM_001255995.3:c.1A=	NP_001242924.1:p.Met1=
NR_045664.2:n.25A=
NR_045665.2:n.25A=