Canonical Allele Identifier: CA2631018533
Gene: IFT140 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1584291_1584292dup , CM000678.2:g.1584291_1584292dup GRCh38
NC_000016.9:g.1634292_1634293dup , CM000678.1:g.1634292_1634293dup GRCh37
NC_000016.8:g.1574293_1574294dup NCBI36
NG_032783.1:g.32821_32822dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.1288_1289dup MANE Select ENSP00000406012.2:p.Phe431AlafsTer?
ENST00000397417.6:c.461_462dup ENSP00000380562.2:p.Leu155CysfsTer?
ENST00000426508.6:c.1288_1289dup ENSP00000406012.2:p.Phe431AlafsTer?
ENST00000439987.6:n.1349_1350dup
NM_014714.3:c.1288_1289dup NP_055529.2:p.Phe431AlafsTer?
XM_005255725.3:c.1288_1289dup XP_005255782.1:p.Phe431AlafsTer?
XM_005255726.2:c.1288_1289dup XP_005255783.1:p.Phe431AlafsTer?
XM_006720989.2:c.1288_1289dup XP_006721052.1:p.Phe431AlafsTer?
XM_006720990.2:c.1288_1289dup XP_006721053.1:p.Phe431AlafsTer?
XM_006720991.2:c.1288_1289dup XP_006721054.1:p.Phe431AlafsTer?
XM_011522766.1:c.1288_1289dup XP_011521068.1:p.Phe431AlafsTer?
XM_011522767.1:c.313_314dup XP_011521069.1:p.Phe106AlafsTer?
XM_011522768.1:c.1288_1289dup XP_011521070.1:p.Phe431AlafsTer?
XM_011522769.1:c.1288_1289dup XP_011521071.1:p.Phe431AlafsTer?
XM_011522771.1:c.1288_1289dup XP_011521073.1:p.Phe431AlafsTer?
XM_011522772.1:c.1288_1289dup XP_011521074.1:p.Phe431AlafsTer?
NR_135176.1:n.59+3706_59+3707dup
XM_005255725.5:c.1288_1289dup XP_005255782.1:p.Phe431AlafsTer?
XM_005255726.4:c.1288_1289dup XP_005255783.1:p.Phe431AlafsTer?
XM_006720990.3:c.1288_1289dup XP_006721053.1:p.Phe431AlafsTer?
XM_006720991.3:c.1288_1289dup XP_006721054.1:p.Phe431AlafsTer?
XM_011522766.3:c.1288_1289dup XP_011521068.1:p.Phe431AlafsTer?
XM_011522767.2:c.313_314dup XP_011521069.1:p.Phe106AlafsTer?
XM_011522769.3:c.1288_1289dup XP_011521071.1:p.Phe431AlafsTer?
XM_011522771.3:c.1288_1289dup XP_011521073.1:p.Phe431AlafsTer?
XM_011522772.3:c.1288_1289dup XP_011521074.1:p.Phe431AlafsTer?
XM_017023910.1:c.1288_1289dup XP_016879399.1:p.Phe431AlafsTer?
XM_017023911.1:c.-410_-409dup XP_016879400.1:n.-410_-409dup
NM_014714.4:c.1288_1289dup MANE Select NP_055529.2:p.Phe431AlafsTer?