Canonical Allele Identifier: CA2201723449
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520184T= , CM000678.2:g.1520184T= GRCh38
NC_000016.9:g.1570185T= , CM000678.1:g.1570185T= GRCh37
NC_000016.8:g.1510186T= NCBI36
NG_032783.1:g.96925A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3820A= MANE Select ENSP00000406012.2:p.Thr1274=
ENST00000361339.9:c.1402A= ENSP00000354895.5:p.Thr468=
ENST00000397417.6:c.*2258A= ENSP00000380562.2:n.*2258A=
ENST00000426508.6:c.3820A= ENSP00000406012.2:p.Thr1274=
ENST00000565298.5:n.3644A=
NM_014714.3:c.3820A= NP_055529.2:p.Thr1274=
XM_006720989.2:c.3820A= XP_006721052.1:p.Thr1274=
XM_006720990.2:c.3820A= XP_006721053.1:p.Thr1274=
XM_006720991.2:c.3820A= XP_006721054.1:p.Thr1274=
XM_006720992.2:c.1453A= XP_006721055.1:p.Thr485=
XM_011522766.1:c.3574A= XP_011521068.1:p.Thr1192=
XM_011522767.1:c.2845A= XP_011521069.1:p.Thr949=
XM_006720990.3:c.3820A= XP_006721053.1:p.Thr1274=
XM_006720991.3:c.3820A= XP_006721054.1:p.Thr1274=
XM_006720992.3:c.1453A= XP_006721055.1:p.Thr485=
XM_011522766.3:c.3574A= XP_011521068.1:p.Thr1192=
XM_011522767.2:c.2845A= XP_011521069.1:p.Thr949=
XM_017023910.1:c.3820A= XP_016879399.1:p.Thr1274=
XM_017023911.1:c.2005A= XP_016879400.1:p.Thr669=
NM_014714.4:c.3820A= MANE Select NP_055529.2:p.Thr1274=