Canonical Allele Identifier: CA2201699085

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525885A= , CM000678.2:g.1525885A=	GRCh38
NC_000016.9:g.1575886A= , CM000678.1:g.1575886A=	GRCh37
NC_000016.8:g.1515887A=	NCBI36
NG_032783.1:g.91224T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2768+2T= MANE Select	ENSP00000406012.2:n.2768+2T=
ENST00000361339.9:c.350+2T=	ENSP00000354895.5:n.350+2T=
ENST00000397417.6:c.*1206+2T=	ENSP00000380562.2:n.*1206+2T=
ENST00000426508.6:c.2768+2T=	ENSP00000406012.2:n.2768+2T=
ENST00000565298.5:n.1997+2T=
ENST00000566818.1:n.483+2T=
NM_014714.3:c.2768+2T=	NP_055529.2:n.2768+2T=
XM_006720989.2:c.2768+2T=	XP_006721052.1:n.2768+2T=
XM_006720990.2:c.2768+2T=	XP_006721053.1:n.2768+2T=
XM_006720991.2:c.2768+2T=	XP_006721054.1:n.2768+2T=
XM_006720992.2:c.401+2T=	XP_006721055.1:n.401+2T=
XM_011522766.1:c.2522+2T=	XP_011521068.1:n.2522+2T=
XM_011522767.1:c.1793+2T=	XP_011521069.1:n.1793+2T=
XM_006720990.3:c.2768+2T=	XP_006721053.1:n.2768+2T=
XM_006720991.3:c.2768+2T=	XP_006721054.1:n.2768+2T=
XM_006720992.3:c.401+2T=	XP_006721055.1:n.401+2T=
XM_011522766.3:c.2522+2T=	XP_011521068.1:n.2522+2T=
XM_011522767.2:c.1793+2T=	XP_011521069.1:n.1793+2T=
XM_017023910.1:c.2768+2T=	XP_016879399.1:n.2768+2T=
XM_017023911.1:c.953+2T=	XP_016879400.1:n.953+2T=
NM_014714.4:c.2768+2T= MANE Select	NP_055529.2:n.2768+2T=