Canonical Allele Identifier: CA2201699086
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1525889A= , CM000678.2:g.1525889A= GRCh38
NC_000016.9:g.1575890A= , CM000678.1:g.1575890A= GRCh37
NC_000016.8:g.1515891A= NCBI36
NG_032783.1:g.91220T=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.2766T= MANE Select ENSP00000406012.2:p.Ser922=
ENST00000361339.9:c.348T= ENSP00000354895.5:p.Ser116=
ENST00000397417.6:c.*1204T= ENSP00000380562.2:n.*1204T=
ENST00000426508.6:c.2766T= ENSP00000406012.2:p.Ser922=
ENST00000565298.5:n.1995T=
ENST00000566818.1:n.481T=
NM_014714.3:c.2766T= NP_055529.2:p.Ser922=
XM_006720989.2:c.2766T= XP_006721052.1:p.Ser922=
XM_006720990.2:c.2766T= XP_006721053.1:p.Ser922=
XM_006720991.2:c.2766T= XP_006721054.1:p.Ser922=
XM_006720992.2:c.399T= XP_006721055.1:p.Ser133=
XM_011522766.1:c.2520T= XP_011521068.1:p.Ser840=
XM_011522767.1:c.1791T= XP_011521069.1:p.Ser597=
XM_006720990.3:c.2766T= XP_006721053.1:p.Ser922=
XM_006720991.3:c.2766T= XP_006721054.1:p.Ser922=
XM_006720992.3:c.399T= XP_006721055.1:p.Ser133=
XM_011522766.3:c.2520T= XP_011521068.1:p.Ser840=
XM_011522767.2:c.1791T= XP_011521069.1:p.Ser597=
XM_017023910.1:c.2766T= XP_016879399.1:p.Ser922=
XM_017023911.1:c.951T= XP_016879400.1:p.Ser317=
NM_014714.4:c.2766T= MANE Select NP_055529.2:p.Ser922=