Canonical Allele Identifier: CA2201723749

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520737G= , CM000678.2:g.1520737G=	GRCh38
NC_000016.9:g.1570738G= , CM000678.1:g.1570738G=	GRCh37
NC_000016.8:g.1510739G=	NCBI36
NG_032783.1:g.96372C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3525C= MANE Select	ENSP00000406012.2:p.Thr1175=
ENST00000361339.9:c.1107C=	ENSP00000354895.5:p.Thr369=
ENST00000397417.6:c.*1963C=	ENSP00000380562.2:n.*1963C=
ENST00000426508.6:c.3525C=	ENSP00000406012.2:p.Thr1175=
ENST00000565298.5:n.3349C=
NM_014714.3:c.3525C=	NP_055529.2:p.Thr1175=
XM_006720989.2:c.3525C=	XP_006721052.1:p.Thr1175=
XM_006720990.2:c.3525C=	XP_006721053.1:p.Thr1175=
XM_006720991.2:c.3525C=	XP_006721054.1:p.Thr1175=
XM_006720992.2:c.1158C=	XP_006721055.1:p.Thr386=
XM_011522766.1:c.3279C=	XP_011521068.1:p.Thr1093=
XM_011522767.1:c.2550C=	XP_011521069.1:p.Thr850=
XM_006720990.3:c.3525C=	XP_006721053.1:p.Thr1175=
XM_006720991.3:c.3525C=	XP_006721054.1:p.Thr1175=
XM_006720992.3:c.1158C=	XP_006721055.1:p.Thr386=
XM_011522766.3:c.3279C=	XP_011521068.1:p.Thr1093=
XM_011522767.2:c.2550C=	XP_011521069.1:p.Thr850=
XM_017023910.1:c.3525C=	XP_016879399.1:p.Thr1175=
XM_017023911.1:c.1710C=	XP_016879400.1:p.Thr570=
NM_014714.4:c.3525C= MANE Select	NP_055529.2:p.Thr1175=