Canonical Allele Identifier: CA2839551441
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1510953dup , CM000678.2:g.1510953dup GRCh38
NC_000016.9:g.1560954dup , CM000678.1:g.1560954dup GRCh37
NC_000016.8:g.1500955dup NCBI36
NG_032783.1:g.106156dup
NG_050910.1:g.22610dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.4380dup MANE Select ENSP00000406012.2:p.Asp1461ArgfsTer?
ENST00000361339.9:c.1962dup ENSP00000354895.5:p.Asp655ArgfsTer?
ENST00000397417.6:c.*2818dup ENSP00000380562.2:n.*2818dup
ENST00000426508.6:c.4380dup ENSP00000406012.2:p.Asp1461ArgfsTer?
ENST00000565298.5:n.4204dup
NM_014714.3:c.4380dup NP_055529.2:p.Asp1461ArgfsTer?
XM_006720989.2:c.4380dup XP_006721052.1:p.Asp1461ArgfsTer?
XM_006720990.2:c.4380dup XP_006721053.1:p.Asp1461ArgfsTer?
XM_006720991.2:c.4380dup XP_006721054.1:p.Asp1461ArgfsTer?
XM_006720992.2:c.2013dup XP_006721055.1:p.Asp672ArgfsTer?
XM_011522766.1:c.4134dup XP_011521068.1:p.Asp1379ArgfsTer?
XM_011522767.1:c.3405dup XP_011521069.1:p.Asp1136ArgfsTer?
XM_006720990.3:c.4380dup XP_006721053.1:p.Asp1461ArgfsTer?
XM_006720991.3:c.4380dup XP_006721054.1:p.Asp1461ArgfsTer?
XM_006720992.3:c.2013dup XP_006721055.1:p.Asp672ArgfsTer?
XM_011522766.3:c.4134dup XP_011521068.1:p.Asp1379ArgfsTer?
XM_011522767.2:c.3405dup XP_011521069.1:p.Asp1136ArgfsTer?
XM_017023910.1:c.4380dup XP_016879399.1:p.Asp1461ArgfsTer?
XM_017023911.1:c.2565dup XP_016879400.1:p.Asp856ArgfsTer?
NM_014714.4:c.4380dup MANE Select NP_055529.2:p.Asp1461ArgfsTer?