Canonical Allele Identifier: CA1746966265

Gene: IFT56

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.139146961C= , CM000669.2:g.139146961C=	GRCh38
NC_000007.13:g.138831707C= , CM000669.1:g.138831707C=	GRCh37
NC_000007.12:g.138482247C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024926.4:c.400-184C= MANE Select	NP_079202.2:n.400-184C=
ENST00000464848.5:c.400-184C= MANE Select	ENSP00000419279.1:n.400-184C=
NM_001144920.2:c.400-184C=	NP_001138392.1:n.400-184C=
NM_001144920.3:c.400-184C=	NP_001138392.1:n.400-184C=
NM_001144923.2:c.307-184C=	NP_001138395.1:n.307-184C=
NM_001144923.3:c.307-184C=	NP_001138395.1:n.307-184C=
NM_001287512.1:c.399+4656C=	NP_001274441.1:n.399+4656C=
NM_001287512.2:c.399+4656C=	NP_001274441.1:n.399+4656C=
NM_001287513.1:c.85-184C=	NP_001274442.1:n.85-184C=
NM_001287513.2:c.85-184C=	NP_001274442.1:n.85-184C=
NM_001318333.1:c.-182-23C=	NP_001305262.1:n.-182-23C=
NM_001318333.2:c.-182-23C=	NP_001305262.1:n.-182-23C=
NM_001321740.1:c.400-184C=	NP_001308669.1:n.400-184C=
NM_001321740.2:c.400-184C=	NP_001308669.1:n.400-184C=
NM_001321741.1:c.399+4656C=	NP_001308670.1:n.399+4656C=
NM_001321741.2:c.399+4656C=	NP_001308670.1:n.399+4656C=
NM_001321742.1:c.400-184C=	NP_001308671.1:n.400-184C=
NM_001321742.2:c.400-184C=	NP_001308671.1:n.400-184C=
NM_024926.3:c.400-184C=	NP_079202.2:n.400-184C=
ENST00000343187.8:c.307-184C=	ENSP00000339135.4:n.307-184C=
ENST00000430935.5:c.400-184C=	ENSP00000410655.1:n.400-184C=
ENST00000468866.1:n.365-184C=
ENST00000474035.6:c.400-184C=	ENSP00000443253.1:n.400-184C=
ENST00000476296.1:c.400-23C=	ENSP00000419639.1:n.400-23C=
ENST00000478836.6:c.399+4656C=	ENSP00000419178.2:n.399+4656C=
ENST00000479132.5:n.411-23C=
ENST00000481482.5:n.478-184C=
ENST00000495038.5:c.399+4656C=	ENSP00000418788.1:n.399+4656C=
XM_005250608.3:c.-182-23C=	XP_005250665.1:n.-182-23C=
XM_006716135.2:c.399+4656C=	XP_006716198.1:n.399+4656C=
XM_011516584.1:c.400-184C=	XP_011514886.1:n.400-184C=