Canonical Allele Identifier: CA2201718456

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511141A= , CM000678.2:g.1511141A=	GRCh38
NC_000016.9:g.1561142A= , CM000678.1:g.1561142A=	GRCh37
NC_000016.8:g.1501143A=	NCBI36
NG_032783.1:g.105968T=
NG_050910.1:g.22798A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4192T= MANE Select	ENSP00000406012.2:p.Phe1398=
ENST00000361339.9:c.1774T=	ENSP00000354895.5:p.Phe592=
ENST00000397417.6:c.*2630T=	ENSP00000380562.2:n.*2630T=
ENST00000426508.6:c.4192T=	ENSP00000406012.2:p.Phe1398=
ENST00000565298.5:n.4016T=
NM_014714.3:c.4192T=	NP_055529.2:p.Phe1398=
XM_006720989.2:c.4192T=	XP_006721052.1:p.Phe1398=
XM_006720990.2:c.4192T=	XP_006721053.1:p.Phe1398=
XM_006720991.2:c.4192T=	XP_006721054.1:p.Phe1398=
XM_006720992.2:c.1825T=	XP_006721055.1:p.Phe609=
XM_011522766.1:c.3946T=	XP_011521068.1:p.Phe1316=
XM_011522767.1:c.3217T=	XP_011521069.1:p.Phe1073=
XM_006720990.3:c.4192T=	XP_006721053.1:p.Phe1398=
XM_006720991.3:c.4192T=	XP_006721054.1:p.Phe1398=
XM_006720992.3:c.1825T=	XP_006721055.1:p.Phe609=
XM_011522766.3:c.3946T=	XP_011521068.1:p.Phe1316=
XM_011522767.2:c.3217T=	XP_011521069.1:p.Phe1073=
XM_017023910.1:c.4192T=	XP_016879399.1:p.Phe1398=
XM_017023911.1:c.2377T=	XP_016879400.1:p.Phe793=
NM_014714.4:c.4192T= MANE Select	NP_055529.2:p.Phe1398=