Canonical Allele Identifier: CA2201723753

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520749C= , CM000678.2:g.1520749C=	GRCh38
NC_000016.9:g.1570750C= , CM000678.1:g.1570750C=	GRCh37
NC_000016.8:g.1510751C=	NCBI36
NG_032783.1:g.96360G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3513G= MANE Select	ENSP00000406012.2:p.Ala1171=
ENST00000361339.9:c.1095G=	ENSP00000354895.5:p.Ala365=
ENST00000397417.6:c.*1951G=	ENSP00000380562.2:n.*1951G=
ENST00000426508.6:c.3513G=	ENSP00000406012.2:p.Ala1171=
ENST00000565298.5:n.3337G=
NM_014714.3:c.3513G=	NP_055529.2:p.Ala1171=
XM_006720989.2:c.3513G=	XP_006721052.1:p.Ala1171=
XM_006720990.2:c.3513G=	XP_006721053.1:p.Ala1171=
XM_006720991.2:c.3513G=	XP_006721054.1:p.Ala1171=
XM_006720992.2:c.1146G=	XP_006721055.1:p.Ala382=
XM_011522766.1:c.3267G=	XP_011521068.1:p.Ala1089=
XM_011522767.1:c.2538G=	XP_011521069.1:p.Ala846=
XM_006720990.3:c.3513G=	XP_006721053.1:p.Ala1171=
XM_006720991.3:c.3513G=	XP_006721054.1:p.Ala1171=
XM_006720992.3:c.1146G=	XP_006721055.1:p.Ala382=
XM_011522766.3:c.3267G=	XP_011521068.1:p.Ala1089=
XM_011522767.2:c.2538G=	XP_011521069.1:p.Ala846=
XM_017023910.1:c.3513G=	XP_016879399.1:p.Ala1171=
XM_017023911.1:c.1698G=	XP_016879400.1:p.Ala566=
NM_014714.4:c.3513G= MANE Select	NP_055529.2:p.Ala1171=