Canonical Allele Identifier: CA2201697809

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523612G= , CM000678.2:g.1523612G=	GRCh38
NC_000016.9:g.1573613G= , CM000678.1:g.1573613G=	GRCh37
NC_000016.8:g.1513614G=	NCBI36
NG_032783.1:g.93497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3359C= MANE Select	ENSP00000406012.2:p.Thr1120=
ENST00000361339.9:c.941C=	ENSP00000354895.5:p.Thr314=
ENST00000397417.6:c.*1797C=	ENSP00000380562.2:n.*1797C=
ENST00000426508.6:c.3359C=	ENSP00000406012.2:p.Thr1120=
ENST00000565298.5:n.3183C=
NM_014714.3:c.3359C=	NP_055529.2:p.Thr1120=
XM_006720989.2:c.3359C=	XP_006721052.1:p.Thr1120=
XM_006720990.2:c.3359C=	XP_006721053.1:p.Thr1120=
XM_006720991.2:c.3359C=	XP_006721054.1:p.Thr1120=
XM_006720992.2:c.992C=	XP_006721055.1:p.Thr331=
XM_011522766.1:c.3113C=	XP_011521068.1:p.Thr1038=
XM_011522767.1:c.2384C=	XP_011521069.1:p.Thr795=
XM_006720990.3:c.3359C=	XP_006721053.1:p.Thr1120=
XM_006720991.3:c.3359C=	XP_006721054.1:p.Thr1120=
XM_006720992.3:c.992C=	XP_006721055.1:p.Thr331=
XM_011522766.3:c.3113C=	XP_011521068.1:p.Thr1038=
XM_011522767.2:c.2384C=	XP_011521069.1:p.Thr795=
XM_017023910.1:c.3359C=	XP_016879399.1:p.Thr1120=
XM_017023911.1:c.1544C=	XP_016879400.1:p.Thr515=
NM_014714.4:c.3359C= MANE Select	NP_055529.2:p.Thr1120=