Canonical Allele Identifier: CA2201718111

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510515G= , CM000678.2:g.1510515G=	GRCh38
NC_000016.9:g.1560516G= , CM000678.1:g.1560516G=	GRCh37
NC_000016.8:g.1500517G=	NCBI36
NG_032783.1:g.106594C=
NG_050910.1:g.22172G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*429C= MANE Select	ENSP00000406012.2:n.*429C=
ENST00000361339.9:c.*429C=	ENSP00000354895.5:n.*429C=
ENST00000397417.6:c.*3256C=	ENSP00000380562.2:n.*3256C=
ENST00000426508.6:c.*429C=	ENSP00000406012.2:n.*429C=
ENST00000565298.5:n.4642C=
NM_014714.3:c.*429C=	NP_055529.2:n.*429C=
XM_006720989.2:c.*429C=	XP_006721052.1:n.*429C=
XM_006720990.2:c.*429C=	XP_006721053.1:n.*429C=
XM_006720991.2:c.*429C=	XP_006721054.1:n.*429C=
XM_006720992.2:c.*429C=	XP_006721055.1:n.*429C=
XM_011522766.1:c.*429C=	XP_011521068.1:n.*429C=
XM_011522767.1:c.*429C=	XP_011521069.1:n.*429C=
XM_006720990.3:c.*429C=	XP_006721053.1:n.*429C=
XM_006720991.3:c.*429C=	XP_006721054.1:n.*429C=
XM_006720992.3:c.*429C=	XP_006721055.1:n.*429C=
XM_011522766.3:c.*429C=	XP_011521068.1:n.*429C=
XM_011522767.2:c.*429C=	XP_011521069.1:n.*429C=
XM_017023910.1:c.*429C=	XP_016879399.1:n.*429C=
XM_017023911.1:c.*429C=	XP_016879400.1:n.*429C=
NM_014714.4:c.*429C= MANE Select	NP_055529.2:n.*429C=