Canonical Allele Identifier: CA2201723306
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1519932G= , CM000678.2:g.1519932G= GRCh38
NC_000016.9:g.1569933G= , CM000678.1:g.1569933G= GRCh37
NC_000016.8:g.1509934G= NCBI36
NG_032783.1:g.97177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3989C= MANE Select ENSP00000406012.2:p.Ala1330=
ENST00000361339.9:c.1571C= ENSP00000354895.5:p.Ala524=
ENST00000397417.6:c.*2427C= ENSP00000380562.2:n.*2427C=
ENST00000426508.6:c.3989C= ENSP00000406012.2:p.Ala1330=
ENST00000565298.5:n.3813C=
ENST00000568837.1:c.107C= ENSP00000458439.1:p.Ala36=
NM_014714.3:c.3989C= NP_055529.2:p.Ala1330=
XM_006720989.2:c.3989C= XP_006721052.1:p.Ala1330=
XM_006720990.2:c.3989C= XP_006721053.1:p.Ala1330=
XM_006720991.2:c.3989C= XP_006721054.1:p.Ala1330=
XM_006720992.2:c.1622C= XP_006721055.1:p.Ala541=
XM_011522766.1:c.3743C= XP_011521068.1:p.Ala1248=
XM_011522767.1:c.3014C= XP_011521069.1:p.Ala1005=
XM_006720990.3:c.3989C= XP_006721053.1:p.Ala1330=
XM_006720991.3:c.3989C= XP_006721054.1:p.Ala1330=
XM_006720992.3:c.1622C= XP_006721055.1:p.Ala541=
XM_011522766.3:c.3743C= XP_011521068.1:p.Ala1248=
XM_011522767.2:c.3014C= XP_011521069.1:p.Ala1005=
XM_017023910.1:c.3989C= XP_016879399.1:p.Ala1330=
XM_017023911.1:c.2174C= XP_016879400.1:p.Ala725=
NM_014714.4:c.3989C= MANE Select NP_055529.2:p.Ala1330=