Canonical Allele Identifier: CA2201718248
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510806G= , CM000678.2:g.1510806G= GRCh38
NC_000016.9:g.1560807G= , CM000678.1:g.1560807G= GRCh37
NC_000016.8:g.1500808G= NCBI36
NG_032783.1:g.106303C=
NG_050910.1:g.22463G=

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.*138C= MANE Select ENSP00000406012.2:n.*138C=
ENST00000361339.9:c.*138C= ENSP00000354895.5:n.*138C=
ENST00000397417.6:c.*2965C= ENSP00000380562.2:n.*2965C=
ENST00000426508.6:c.*138C= ENSP00000406012.2:n.*138C=
ENST00000565298.5:n.4351C=
NM_014714.3:c.*138C= NP_055529.2:n.*138C=
XM_006720989.2:c.*138C= XP_006721052.1:n.*138C=
XM_006720990.2:c.*138C= XP_006721053.1:n.*138C=
XM_006720991.2:c.*138C= XP_006721054.1:n.*138C=
XM_006720992.2:c.*138C= XP_006721055.1:n.*138C=
XM_011522766.1:c.*138C= XP_011521068.1:n.*138C=
XM_011522767.1:c.*138C= XP_011521069.1:n.*138C=
XM_006720990.3:c.*138C= XP_006721053.1:n.*138C=
XM_006720991.3:c.*138C= XP_006721054.1:n.*138C=
XM_006720992.3:c.*138C= XP_006721055.1:n.*138C=
XM_011522766.3:c.*138C= XP_011521068.1:n.*138C=
XM_011522767.2:c.*138C= XP_011521069.1:n.*138C=
XM_017023910.1:c.*138C= XP_016879399.1:n.*138C=
XM_017023911.1:c.*138C= XP_016879400.1:n.*138C=
NM_014714.4:c.*138C= MANE Select NP_055529.2:n.*138C=