Canonical Allele Identifier: CA1746966223

Gene: IFT56

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.139146878G= , CM000669.2:g.139146878G=	GRCh38
NC_000007.13:g.138831624G= , CM000669.1:g.138831624G=	GRCh37
NC_000007.12:g.138482164G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343187.8:c.307-267G=	ENSP00000339135.4:n.307-267G=
ENST00000430935.5:c.400-267G=	ENSP00000410655.1:n.400-267G=
ENST00000464848.5:c.400-267G= MANE Select	ENSP00000419279.1:n.400-267G=
ENST00000468866.1:n.365-267G=
ENST00000474035.6:c.400-267G=	ENSP00000443253.1:n.400-267G=
ENST00000476296.1:c.400-106G=	ENSP00000419639.1:n.400-106G=
ENST00000478836.6:c.399+4573G=	ENSP00000419178.2:n.399+4573G=
ENST00000479132.5:n.411-106G=
ENST00000481482.5:n.478-267G=
ENST00000495038.5:c.399+4573G=	ENSP00000418788.1:n.399+4573G=
NM_001144920.2:c.400-267G=	NP_001138392.1:n.400-267G=
NM_001144923.2:c.307-267G=	NP_001138395.1:n.307-267G=
NM_001287512.1:c.399+4573G=	NP_001274441.1:n.399+4573G=
NM_001287513.1:c.85-267G=	NP_001274442.1:n.85-267G=
NM_024926.3:c.400-267G=	NP_079202.2:n.400-267G=
XM_005250608.3:c.-182-106G=	XP_005250665.1:n.-182-106G=
XM_006716135.2:c.399+4573G=	XP_006716198.1:n.399+4573G=
XM_011516584.1:c.400-267G=	XP_011514886.1:n.400-267G=
NM_001318333.1:c.-182-106G=	NP_001305262.1:n.-182-106G=
NM_001321740.1:c.400-267G=	NP_001308669.1:n.400-267G=
NM_001321741.1:c.399+4573G=	NP_001308670.1:n.399+4573G=
NM_001321742.1:c.400-267G=	NP_001308671.1:n.400-267G=
NM_024926.4:c.400-267G= MANE Select	NP_079202.2:n.400-267G=
NM_001144923.3:c.307-267G=	NP_001138395.1:n.307-267G=
NM_001287512.2:c.399+4573G=	NP_001274441.1:n.399+4573G=
NM_001287513.2:c.85-267G=	NP_001274442.1:n.85-267G=
NM_001318333.2:c.-182-106G=	NP_001305262.1:n.-182-106G=
NM_001321740.2:c.400-267G=	NP_001308669.1:n.400-267G=
NM_001321741.2:c.399+4573G=	NP_001308670.1:n.399+4573G=
NM_001144920.3:c.400-267G=	NP_001138392.1:n.400-267G=
NM_001321742.2:c.400-267G=	NP_001308671.1:n.400-267G=