Canonical Allele Identifier: CA2201723450
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520185G= , CM000678.2:g.1520185G= GRCh38
NC_000016.9:g.1570186G= , CM000678.1:g.1570186G= GRCh37
NC_000016.8:g.1510187G= NCBI36
NG_032783.1:g.96924C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3819C= MANE Select ENSP00000406012.2:p.Tyr1273=
ENST00000361339.9:c.1401C= ENSP00000354895.5:p.Tyr467=
ENST00000397417.6:c.*2257C= ENSP00000380562.2:n.*2257C=
ENST00000426508.6:c.3819C= ENSP00000406012.2:p.Tyr1273=
ENST00000565298.5:n.3643C=
NM_014714.3:c.3819C= NP_055529.2:p.Tyr1273=
XM_006720989.2:c.3819C= XP_006721052.1:p.Tyr1273=
XM_006720990.2:c.3819C= XP_006721053.1:p.Tyr1273=
XM_006720991.2:c.3819C= XP_006721054.1:p.Tyr1273=
XM_006720992.2:c.1452C= XP_006721055.1:p.Tyr484=
XM_011522766.1:c.3573C= XP_011521068.1:p.Tyr1191=
XM_011522767.1:c.2844C= XP_011521069.1:p.Tyr948=
XM_006720990.3:c.3819C= XP_006721053.1:p.Tyr1273=
XM_006720991.3:c.3819C= XP_006721054.1:p.Tyr1273=
XM_006720992.3:c.1452C= XP_006721055.1:p.Tyr484=
XM_011522766.3:c.3573C= XP_011521068.1:p.Tyr1191=
XM_011522767.2:c.2844C= XP_011521069.1:p.Tyr948=
XM_017023910.1:c.3819C= XP_016879399.1:p.Tyr1273=
XM_017023911.1:c.2004C= XP_016879400.1:p.Tyr668=
NM_014714.4:c.3819C= MANE Select NP_055529.2:p.Tyr1273=