Canonical Allele Identifier: CA2201731293
Gene: IFT140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1566155_1566156delinsTC , CM000678.2:g.1566155_1566156delinsTC GRCh38
NC_000016.9:g.1616156_1616157delinsTC , CM000678.1:g.1616156_1616157delinsTC GRCh37
NC_000016.8:g.1556157_1556158delinsTC NCBI36
NG_032783.1:g.50953_50954delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000426508.7:c.1901+5_1901+6delinsGA MANE Select ENSP00000406012.2:n.1901+5_1901+6delinsGA
ENST00000397417.6:c.*453+5_*453+6delinsGA ENSP00000380562.2:n.*453+5_*453+6delinsGA
ENST00000426508.6:c.1901+5_1901+6delinsGA ENSP00000406012.2:n.1901+5_1901+6delinsGA
ENST00000439987.6:n.1962+5_1962+6delinsGA
ENST00000565298.5:n.589+5_589+6delinsGA
NM_014714.3:c.1901+5_1901+6delinsGA NP_055529.2:n.1901+5_1901+6delinsGA
XM_005255725.3:c.1901+5_1901+6delinsGA XP_005255782.1:n.1901+5_1901+6delinsGA
XM_005255726.2:c.1901+5_1901+6delinsGA XP_005255783.1:n.1901+5_1901+6delinsGA
XM_006720989.2:c.1901+5_1901+6delinsGA XP_006721052.1:n.1901+5_1901+6delinsGA
XM_006720990.2:c.1901+5_1901+6delinsGA XP_006721053.1:n.1901+5_1901+6delinsGA
XM_006720991.2:c.1901+5_1901+6delinsGA XP_006721054.1:n.1901+5_1901+6delinsGA
XM_011522766.1:c.1655+5_1655+6delinsGA XP_011521068.1:n.1655+5_1655+6delinsGA
XM_011522767.1:c.926+5_926+6delinsGA XP_011521069.1:n.926+5_926+6delinsGA
XM_011522768.1:c.1901+5_1901+6delinsGA XP_011521070.1:n.1901+5_1901+6delinsGA
XM_011522769.1:c.1901+5_1901+6delinsGA XP_011521071.1:n.1901+5_1901+6delinsGA
XM_011522771.1:c.1901+5_1901+6delinsGA XP_011521073.1:n.1901+5_1901+6delinsGA
XM_011522772.1:c.1901+5_1901+6delinsGA XP_011521074.1:n.1901+5_1901+6delinsGA
XM_005255725.5:c.1901+5_1901+6delinsGA XP_005255782.1:n.1901+5_1901+6delinsGA
XM_005255726.4:c.1901+5_1901+6delinsGA XP_005255783.1:n.1901+5_1901+6delinsGA
XM_006720990.3:c.1901+5_1901+6delinsGA XP_006721053.1:n.1901+5_1901+6delinsGA
XM_006720991.3:c.1901+5_1901+6delinsGA XP_006721054.1:n.1901+5_1901+6delinsGA
XM_011522766.3:c.1655+5_1655+6delinsGA XP_011521068.1:n.1655+5_1655+6delinsGA
XM_011522767.2:c.926+5_926+6delinsGA XP_011521069.1:n.926+5_926+6delinsGA
XM_011522769.3:c.1901+5_1901+6delinsGA XP_011521071.1:n.1901+5_1901+6delinsGA
XM_011522771.3:c.1901+5_1901+6delinsGA XP_011521073.1:n.1901+5_1901+6delinsGA
XM_011522772.3:c.1901+5_1901+6delinsGA XP_011521074.1:n.1901+5_1901+6delinsGA
XM_017023910.1:c.1901+5_1901+6delinsGA XP_016879399.1:n.1901+5_1901+6delinsGA
XM_017023911.1:c.86+5_86+6delinsGA XP_016879400.1:n.86+5_86+6delinsGA
NM_014714.4:c.1901+5_1901+6delinsGA MANE Select NP_055529.2:n.1901+5_1901+6delinsGA