Canonical Allele Identifier: CA2201718352

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510971C= , CM000678.2:g.1510971C=	GRCh38
NC_000016.9:g.1560972C= , CM000678.1:g.1560972C=	GRCh37
NC_000016.8:g.1500973C=	NCBI36
NG_032783.1:g.106138G=
NG_050910.1:g.22628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4362G= MANE Select	ENSP00000406012.2:p.Val1454=
ENST00000361339.9:c.1944G=	ENSP00000354895.5:p.Val648=
ENST00000397417.6:c.*2800G=	ENSP00000380562.2:n.*2800G=
ENST00000426508.6:c.4362G=	ENSP00000406012.2:p.Val1454=
ENST00000565298.5:n.4186G=
NM_014714.3:c.4362G=	NP_055529.2:p.Val1454=
XM_006720989.2:c.4362G=	XP_006721052.1:p.Val1454=
XM_006720990.2:c.4362G=	XP_006721053.1:p.Val1454=
XM_006720991.2:c.4362G=	XP_006721054.1:p.Val1454=
XM_006720992.2:c.1995G=	XP_006721055.1:p.Val665=
XM_011522766.1:c.4116G=	XP_011521068.1:p.Val1372=
XM_011522767.1:c.3387G=	XP_011521069.1:p.Val1129=
XM_006720990.3:c.4362G=	XP_006721053.1:p.Val1454=
XM_006720991.3:c.4362G=	XP_006721054.1:p.Val1454=
XM_006720992.3:c.1995G=	XP_006721055.1:p.Val665=
XM_011522766.3:c.4116G=	XP_011521068.1:p.Val1372=
XM_011522767.2:c.3387G=	XP_011521069.1:p.Val1129=
XM_017023910.1:c.4362G=	XP_016879399.1:p.Val1454=
XM_017023911.1:c.2547G=	XP_016879400.1:p.Val849=
NM_014714.4:c.4362G= MANE Select	NP_055529.2:p.Val1454=