Canonical Allele Identifier: CA2201699150
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1525983A= , CM000678.2:g.1525983A= GRCh38
NC_000016.9:g.1575984A= , CM000678.1:g.1575984A= GRCh37
NC_000016.8:g.1515985A= NCBI36
NG_032783.1:g.91126T=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.2672T= MANE Select ENSP00000406012.2:p.Val891=
ENST00000361339.9:c.254T= ENSP00000354895.5:p.Val85=
ENST00000397417.6:c.*1110T= ENSP00000380562.2:n.*1110T=
ENST00000426508.6:c.2672T= ENSP00000406012.2:p.Val891=
ENST00000565298.5:n.1901T=
ENST00000566818.1:n.387T=
NM_014714.3:c.2672T= NP_055529.2:p.Val891=
XM_006720989.2:c.2672T= XP_006721052.1:p.Val891=
XM_006720990.2:c.2672T= XP_006721053.1:p.Val891=
XM_006720991.2:c.2672T= XP_006721054.1:p.Val891=
XM_006720992.2:c.305T= XP_006721055.1:p.Val102=
XM_011522766.1:c.2426T= XP_011521068.1:p.Val809=
XM_011522767.1:c.1697T= XP_011521069.1:p.Val566=
XM_006720990.3:c.2672T= XP_006721053.1:p.Val891=
XM_006720991.3:c.2672T= XP_006721054.1:p.Val891=
XM_006720992.3:c.305T= XP_006721055.1:p.Val102=
XM_011522766.3:c.2426T= XP_011521068.1:p.Val809=
XM_011522767.2:c.1697T= XP_011521069.1:p.Val566=
XM_017023910.1:c.2672T= XP_016879399.1:p.Val891=
XM_017023911.1:c.857T= XP_016879400.1:p.Val286=
NM_014714.4:c.2672T= MANE Select NP_055529.2:p.Val891=