Canonical Allele Identifier: CA2201697819
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1523635G= , CM000678.2:g.1523635G= GRCh38
NC_000016.9:g.1573636G= , CM000678.1:g.1573636G= GRCh37
NC_000016.8:g.1513637G= NCBI36
NG_032783.1:g.93474C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3336C= MANE Select ENSP00000406012.2:p.Leu1112=
ENST00000361339.9:c.918C= ENSP00000354895.5:p.Leu306=
ENST00000397417.6:c.*1774C= ENSP00000380562.2:n.*1774C=
ENST00000426508.6:c.3336C= ENSP00000406012.2:p.Leu1112=
ENST00000565298.5:n.3160C=
NM_014714.3:c.3336C= NP_055529.2:p.Leu1112=
XM_006720989.2:c.3336C= XP_006721052.1:p.Leu1112=
XM_006720990.2:c.3336C= XP_006721053.1:p.Leu1112=
XM_006720991.2:c.3336C= XP_006721054.1:p.Leu1112=
XM_006720992.2:c.969C= XP_006721055.1:p.Leu323=
XM_011522766.1:c.3090C= XP_011521068.1:p.Leu1030=
XM_011522767.1:c.2361C= XP_011521069.1:p.Leu787=
XM_006720990.3:c.3336C= XP_006721053.1:p.Leu1112=
XM_006720991.3:c.3336C= XP_006721054.1:p.Leu1112=
XM_006720992.3:c.969C= XP_006721055.1:p.Leu323=
XM_011522766.3:c.3090C= XP_011521068.1:p.Leu1030=
XM_011522767.2:c.2361C= XP_011521069.1:p.Leu787=
XM_017023910.1:c.3336C= XP_016879399.1:p.Leu1112=
XM_017023911.1:c.1521C= XP_016879400.1:p.Leu507=
NM_014714.4:c.3336C= MANE Select NP_055529.2:p.Leu1112=