Canonical Allele Identifier: CA394224900
Gene: IFT140 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520706C>T , CM000678.2:g.1520706C>T GRCh38
NC_000016.9:g.1570707C>T , CM000678.1:g.1570707C>T GRCh37
NC_000016.8:g.1510708C>T NCBI36
NG_032783.1:g.96403G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3556G>A MANE Select ENSP00000406012.2:p.Glu1186Lys
ENST00000361339.9:c.1138G>A ENSP00000354895.5:p.Glu380Lys
ENST00000397417.6:c.*1994G>A ENSP00000380562.2:n.*1994G>A
ENST00000426508.6:c.3556G>A ENSP00000406012.2:p.Glu1186Lys
ENST00000565298.5:n.3380G>A
NM_014714.3:c.3556G>A NP_055529.2:p.Glu1186Lys
XM_006720989.2:c.3556G>A XP_006721052.1:p.Glu1186Lys
XM_006720990.2:c.3556G>A XP_006721053.1:p.Glu1186Lys
XM_006720991.2:c.3556G>A XP_006721054.1:p.Glu1186Lys
XM_006720992.2:c.1189G>A XP_006721055.1:p.Glu397Lys
XM_011522766.1:c.3310G>A XP_011521068.1:p.Glu1104Lys
XM_011522767.1:c.2581G>A XP_011521069.1:p.Glu861Lys
XM_006720990.3:c.3556G>A XP_006721053.1:p.Glu1186Lys
XM_006720991.3:c.3556G>A XP_006721054.1:p.Glu1186Lys
XM_006720992.3:c.1189G>A XP_006721055.1:p.Glu397Lys
XM_011522766.3:c.3310G>A XP_011521068.1:p.Glu1104Lys
XM_011522767.2:c.2581G>A XP_011521069.1:p.Glu861Lys
XM_017023910.1:c.3556G>A XP_016879399.1:p.Glu1186Lys
XM_017023911.1:c.1741G>A XP_016879400.1:p.Glu581Lys
NM_014714.4:c.3556G>A MANE Select NP_055529.2:p.Glu1186Lys