Canonical Allele Identifier: CA2201731341

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1566237C= , CM000678.2:g.1566237C=	GRCh38
NC_000016.9:g.1616238C= , CM000678.1:g.1616238C=	GRCh37
NC_000016.8:g.1556239C=	NCBI36
NG_032783.1:g.50872G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.1825G= MANE Select	ENSP00000406012.2:p.Val609=
ENST00000397417.6:c.*377G=	ENSP00000380562.2:n.*377G=
ENST00000426508.6:c.1825G=	ENSP00000406012.2:p.Val609=
ENST00000439987.6:n.1886G=
ENST00000565298.5:n.513G=
NM_014714.3:c.1825G=	NP_055529.2:p.Val609=
XM_005255725.3:c.1825G=	XP_005255782.1:p.Val609=
XM_005255726.2:c.1825G=	XP_005255783.1:p.Val609=
XM_006720989.2:c.1825G=	XP_006721052.1:p.Val609=
XM_006720990.2:c.1825G=	XP_006721053.1:p.Val609=
XM_006720991.2:c.1825G=	XP_006721054.1:p.Val609=
XM_011522766.1:c.1579G=	XP_011521068.1:p.Val527=
XM_011522767.1:c.850G=	XP_011521069.1:p.Val284=
XM_011522768.1:c.1825G=	XP_011521070.1:p.Val609=
XM_011522769.1:c.1825G=	XP_011521071.1:p.Val609=
XM_011522771.1:c.1825G=	XP_011521073.1:p.Val609=
XM_011522772.1:c.1825G=	XP_011521074.1:p.Val609=
XM_005255725.5:c.1825G=	XP_005255782.1:p.Val609=
XM_005255726.4:c.1825G=	XP_005255783.1:p.Val609=
XM_006720990.3:c.1825G=	XP_006721053.1:p.Val609=
XM_006720991.3:c.1825G=	XP_006721054.1:p.Val609=
XM_011522766.3:c.1579G=	XP_011521068.1:p.Val527=
XM_011522767.2:c.850G=	XP_011521069.1:p.Val284=
XM_011522769.3:c.1825G=	XP_011521071.1:p.Val609=
XM_011522771.3:c.1825G=	XP_011521073.1:p.Val609=
XM_011522772.3:c.1825G=	XP_011521074.1:p.Val609=
XM_017023910.1:c.1825G=	XP_016879399.1:p.Val609=
XM_017023911.1:c.10G=	XP_016879400.1:p.Val4=
NM_014714.4:c.1825G= MANE Select	NP_055529.2:p.Val609=