Canonical Allele Identifier: CA2201697824

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523645G= , CM000678.2:g.1523645G=	GRCh38
NC_000016.9:g.1573646G= , CM000678.1:g.1573646G=	GRCh37
NC_000016.8:g.1513647G=	NCBI36
NG_032783.1:g.93464C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3326C= MANE Select	ENSP00000406012.2:p.Ala1109=
ENST00000361339.9:c.908C=	ENSP00000354895.5:p.Ala303=
ENST00000397417.6:c.*1764C=	ENSP00000380562.2:n.*1764C=
ENST00000426508.6:c.3326C=	ENSP00000406012.2:p.Ala1109=
ENST00000565298.5:n.3150C=
NM_014714.3:c.3326C=	NP_055529.2:p.Ala1109=
XM_006720989.2:c.3326C=	XP_006721052.1:p.Ala1109=
XM_006720990.2:c.3326C=	XP_006721053.1:p.Ala1109=
XM_006720991.2:c.3326C=	XP_006721054.1:p.Ala1109=
XM_006720992.2:c.959C=	XP_006721055.1:p.Ala320=
XM_011522766.1:c.3080C=	XP_011521068.1:p.Ala1027=
XM_011522767.1:c.2351C=	XP_011521069.1:p.Ala784=
XM_006720990.3:c.3326C=	XP_006721053.1:p.Ala1109=
XM_006720991.3:c.3326C=	XP_006721054.1:p.Ala1109=
XM_006720992.3:c.959C=	XP_006721055.1:p.Ala320=
XM_011522766.3:c.3080C=	XP_011521068.1:p.Ala1027=
XM_011522767.2:c.2351C=	XP_011521069.1:p.Ala784=
XM_017023910.1:c.3326C=	XP_016879399.1:p.Ala1109=
XM_017023911.1:c.1511C=	XP_016879400.1:p.Ala504=
NM_014714.4:c.3326C= MANE Select	NP_055529.2:p.Ala1109=