Canonical Allele Identifier: CA394224317
Gene: IFT140 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520181T>A , CM000678.2:g.1520181T>A GRCh38
NC_000016.9:g.1570182T>A , CM000678.1:g.1570182T>A GRCh37
NC_000016.8:g.1510183T>A NCBI36
NG_032783.1:g.96928A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.3823A>T MANE Select ENSP00000406012.2:p.Lys1275Ter
ENST00000361339.9:c.1405A>T ENSP00000354895.5:p.Lys469Ter
ENST00000397417.6:c.*2261A>T ENSP00000380562.2:n.*2261A>T
ENST00000426508.6:c.3823A>T ENSP00000406012.2:p.Lys1275Ter
ENST00000565298.5:n.3647A>T
NM_014714.3:c.3823A>T NP_055529.2:p.Lys1275Ter
XM_006720989.2:c.3823A>T XP_006721052.1:p.Lys1275Ter
XM_006720990.2:c.3823A>T XP_006721053.1:p.Lys1275Ter
XM_006720991.2:c.3823A>T XP_006721054.1:p.Lys1275Ter
XM_006720992.2:c.1456A>T XP_006721055.1:p.Lys486Ter
XM_011522766.1:c.3577A>T XP_011521068.1:p.Lys1193Ter
XM_011522767.1:c.2848A>T XP_011521069.1:p.Lys950Ter
XM_006720990.3:c.3823A>T XP_006721053.1:p.Lys1275Ter
XM_006720991.3:c.3823A>T XP_006721054.1:p.Lys1275Ter
XM_006720992.3:c.1456A>T XP_006721055.1:p.Lys486Ter
XM_011522766.3:c.3577A>T XP_011521068.1:p.Lys1193Ter
XM_011522767.2:c.2848A>T XP_011521069.1:p.Lys950Ter
XM_017023910.1:c.3823A>T XP_016879399.1:p.Lys1275Ter
XM_017023911.1:c.2008A>T XP_016879400.1:p.Lys670Ter
NM_014714.4:c.3823A>T MANE Select NP_055529.2:p.Lys1275Ter