Canonical Allele Identifier: CA2201697801
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1523594A= , CM000678.2:g.1523594A= GRCh38
NC_000016.9:g.1573595A= , CM000678.1:g.1573595A= GRCh37
NC_000016.8:g.1513596A= NCBI36
NG_032783.1:g.93515T=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.3377T= MANE Select ENSP00000406012.2:p.Leu1126=
ENST00000361339.9:c.959T= ENSP00000354895.5:p.Leu320=
ENST00000397417.6:c.*1815T= ENSP00000380562.2:n.*1815T=
ENST00000426508.6:c.3377T= ENSP00000406012.2:p.Leu1126=
ENST00000565298.5:n.3201T=
NM_014714.3:c.3377T= NP_055529.2:p.Leu1126=
XM_006720989.2:c.3377T= XP_006721052.1:p.Leu1126=
XM_006720990.2:c.3377T= XP_006721053.1:p.Leu1126=
XM_006720991.2:c.3377T= XP_006721054.1:p.Leu1126=
XM_006720992.2:c.1010T= XP_006721055.1:p.Leu337=
XM_011522766.1:c.3131T= XP_011521068.1:p.Leu1044=
XM_011522767.1:c.2402T= XP_011521069.1:p.Leu801=
XM_006720990.3:c.3377T= XP_006721053.1:p.Leu1126=
XM_006720991.3:c.3377T= XP_006721054.1:p.Leu1126=
XM_006720992.3:c.1010T= XP_006721055.1:p.Leu337=
XM_011522766.3:c.3131T= XP_011521068.1:p.Leu1044=
XM_011522767.2:c.2402T= XP_011521069.1:p.Leu801=
XM_017023910.1:c.3377T= XP_016879399.1:p.Leu1126=
XM_017023911.1:c.1562T= XP_016879400.1:p.Leu521=
NM_014714.4:c.3377T= MANE Select NP_055529.2:p.Leu1126=