Canonical Allele Identifier: CA2201699149

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525980G= , CM000678.2:g.1525980G=	GRCh38
NC_000016.9:g.1575981G= , CM000678.1:g.1575981G=	GRCh37
NC_000016.8:g.1515982G=	NCBI36
NG_032783.1:g.91129C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2675C= MANE Select	ENSP00000406012.2:p.Ala892=
ENST00000361339.9:c.257C=	ENSP00000354895.5:p.Ala86=
ENST00000397417.6:c.*1113C=	ENSP00000380562.2:n.*1113C=
ENST00000426508.6:c.2675C=	ENSP00000406012.2:p.Ala892=
ENST00000565298.5:n.1904C=
ENST00000566818.1:n.390C=
NM_014714.3:c.2675C=	NP_055529.2:p.Ala892=
XM_006720989.2:c.2675C=	XP_006721052.1:p.Ala892=
XM_006720990.2:c.2675C=	XP_006721053.1:p.Ala892=
XM_006720991.2:c.2675C=	XP_006721054.1:p.Ala892=
XM_006720992.2:c.308C=	XP_006721055.1:p.Ala103=
XM_011522766.1:c.2429C=	XP_011521068.1:p.Ala810=
XM_011522767.1:c.1700C=	XP_011521069.1:p.Ala567=
XM_006720990.3:c.2675C=	XP_006721053.1:p.Ala892=
XM_006720991.3:c.2675C=	XP_006721054.1:p.Ala892=
XM_006720992.3:c.308C=	XP_006721055.1:p.Ala103=
XM_011522766.3:c.2429C=	XP_011521068.1:p.Ala810=
XM_011522767.2:c.1700C=	XP_011521069.1:p.Ala567=
XM_017023910.1:c.2675C=	XP_016879399.1:p.Ala892=
XM_017023911.1:c.860C=	XP_016879400.1:p.Ala287=
NM_014714.4:c.2675C= MANE Select	NP_055529.2:p.Ala892=