Canonical Allele Identifier: CA2201699147
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1525978C= , CM000678.2:g.1525978C= GRCh38
NC_000016.9:g.1575979C= , CM000678.1:g.1575979C= GRCh37
NC_000016.8:g.1515980C= NCBI36
NG_032783.1:g.91131G=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.2677G= MANE Select ENSP00000406012.2:p.Glu893=
ENST00000361339.9:c.259G= ENSP00000354895.5:p.Glu87=
ENST00000397417.6:c.*1115G= ENSP00000380562.2:n.*1115G=
ENST00000426508.6:c.2677G= ENSP00000406012.2:p.Glu893=
ENST00000565298.5:n.1906G=
ENST00000566818.1:n.392G=
NM_014714.3:c.2677G= NP_055529.2:p.Glu893=
XM_006720989.2:c.2677G= XP_006721052.1:p.Glu893=
XM_006720990.2:c.2677G= XP_006721053.1:p.Glu893=
XM_006720991.2:c.2677G= XP_006721054.1:p.Glu893=
XM_006720992.2:c.310G= XP_006721055.1:p.Glu104=
XM_011522766.1:c.2431G= XP_011521068.1:p.Glu811=
XM_011522767.1:c.1702G= XP_011521069.1:p.Glu568=
XM_006720990.3:c.2677G= XP_006721053.1:p.Glu893=
XM_006720991.3:c.2677G= XP_006721054.1:p.Glu893=
XM_006720992.3:c.310G= XP_006721055.1:p.Glu104=
XM_011522766.3:c.2431G= XP_011521068.1:p.Glu811=
XM_011522767.2:c.1702G= XP_011521069.1:p.Glu568=
XM_017023910.1:c.2677G= XP_016879399.1:p.Glu893=
XM_017023911.1:c.862G= XP_016879400.1:p.Glu288=
NM_014714.4:c.2677G= MANE Select NP_055529.2:p.Glu893=