Canonical Allele Identifier: CA2201723309

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1519935A= , CM000678.2:g.1519935A=	GRCh38
NC_000016.9:g.1569936A= , CM000678.1:g.1569936A=	GRCh37
NC_000016.8:g.1509937A=	NCBI36
NG_032783.1:g.97174T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3986T= MANE Select	ENSP00000406012.2:p.Leu1329=
ENST00000361339.9:c.1568T=	ENSP00000354895.5:p.Leu523=
ENST00000397417.6:c.*2424T=	ENSP00000380562.2:n.*2424T=
ENST00000426508.6:c.3986T=	ENSP00000406012.2:p.Leu1329=
ENST00000565298.5:n.3810T=
ENST00000568837.1:c.104T=	ENSP00000458439.1:p.Leu35=
NM_014714.3:c.3986T=	NP_055529.2:p.Leu1329=
XM_006720989.2:c.3986T=	XP_006721052.1:p.Leu1329=
XM_006720990.2:c.3986T=	XP_006721053.1:p.Leu1329=
XM_006720991.2:c.3986T=	XP_006721054.1:p.Leu1329=
XM_006720992.2:c.1619T=	XP_006721055.1:p.Leu540=
XM_011522766.1:c.3740T=	XP_011521068.1:p.Leu1247=
XM_011522767.1:c.3011T=	XP_011521069.1:p.Leu1004=
XM_006720990.3:c.3986T=	XP_006721053.1:p.Leu1329=
XM_006720991.3:c.3986T=	XP_006721054.1:p.Leu1329=
XM_006720992.3:c.1619T=	XP_006721055.1:p.Leu540=
XM_011522766.3:c.3740T=	XP_011521068.1:p.Leu1247=
XM_011522767.2:c.3011T=	XP_011521069.1:p.Leu1004=
XM_017023910.1:c.3986T=	XP_016879399.1:p.Leu1329=
XM_017023911.1:c.2171T=	XP_016879400.1:p.Leu724=
NM_014714.4:c.3986T= MANE Select	NP_055529.2:p.Leu1329=