Canonical Allele Identifier: CA2201723442
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520174C= , CM000678.2:g.1520174C= GRCh38
NC_000016.9:g.1570175C= , CM000678.1:g.1570175C= GRCh37
NC_000016.8:g.1510176C= NCBI36
NG_032783.1:g.96935G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3830G= MANE Select ENSP00000406012.2:p.Arg1277=
ENST00000361339.9:c.1412G= ENSP00000354895.5:p.Arg471=
ENST00000397417.6:c.*2268G= ENSP00000380562.2:n.*2268G=
ENST00000426508.6:c.3830G= ENSP00000406012.2:p.Arg1277=
ENST00000565298.5:n.3654G=
NM_014714.3:c.3830G= NP_055529.2:p.Arg1277=
XM_006720989.2:c.3830G= XP_006721052.1:p.Arg1277=
XM_006720990.2:c.3830G= XP_006721053.1:p.Arg1277=
XM_006720991.2:c.3830G= XP_006721054.1:p.Arg1277=
XM_006720992.2:c.1463G= XP_006721055.1:p.Arg488=
XM_011522766.1:c.3584G= XP_011521068.1:p.Arg1195=
XM_011522767.1:c.2855G= XP_011521069.1:p.Arg952=
XM_006720990.3:c.3830G= XP_006721053.1:p.Arg1277=
XM_006720991.3:c.3830G= XP_006721054.1:p.Arg1277=
XM_006720992.3:c.1463G= XP_006721055.1:p.Arg488=
XM_011522766.3:c.3584G= XP_011521068.1:p.Arg1195=
XM_011522767.2:c.2855G= XP_011521069.1:p.Arg952=
XM_017023910.1:c.3830G= XP_016879399.1:p.Arg1277=
XM_017023911.1:c.2015G= XP_016879400.1:p.Arg672=
NM_014714.4:c.3830G= MANE Select NP_055529.2:p.Arg1277=