Canonical Allele Identifier: CA2631006600
Gene: IFT140 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1520891_1520898del , CM000678.2:g.1520891_1520898del GRCh38
NC_000016.9:g.1570892_1570899del , CM000678.1:g.1570892_1570899del GRCh37
NC_000016.8:g.1510893_1510900del NCBI36
NG_032783.1:g.96214_96221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.3454-87_3454-80del MANE Select ENSP00000406012.2:n.3454-87_3454-80del
ENST00000361339.9:c.1036-87_1036-80del ENSP00000354895.5:n.1036-87_1036-80del
ENST00000397417.6:c.*1892-87_*1892-80del ENSP00000380562.2:n.*1892-87_*1892-80del
ENST00000426508.6:c.3454-87_3454-80del ENSP00000406012.2:n.3454-87_3454-80del
ENST00000565298.5:n.3278-87_3278-80del
NM_014714.3:c.3454-87_3454-80del NP_055529.2:n.3454-87_3454-80del
XM_006720989.2:c.3454-87_3454-80del XP_006721052.1:n.3454-87_3454-80del
XM_006720990.2:c.3454-87_3454-80del XP_006721053.1:n.3454-87_3454-80del
XM_006720991.2:c.3454-87_3454-80del XP_006721054.1:n.3454-87_3454-80del
XM_006720992.2:c.1087-87_1087-80del XP_006721055.1:n.1087-87_1087-80del
XM_011522766.1:c.3208-87_3208-80del XP_011521068.1:n.3208-87_3208-80del
XM_011522767.1:c.2479-87_2479-80del XP_011521069.1:n.2479-87_2479-80del
XM_006720990.3:c.3454-87_3454-80del XP_006721053.1:n.3454-87_3454-80del
XM_006720991.3:c.3454-87_3454-80del XP_006721054.1:n.3454-87_3454-80del
XM_006720992.3:c.1087-87_1087-80del XP_006721055.1:n.1087-87_1087-80del
XM_011522766.3:c.3208-87_3208-80del XP_011521068.1:n.3208-87_3208-80del
XM_011522767.2:c.2479-87_2479-80del XP_011521069.1:n.2479-87_2479-80del
XM_017023910.1:c.3454-87_3454-80del XP_016879399.1:n.3454-87_3454-80del
XM_017023911.1:c.1639-87_1639-80del XP_016879400.1:n.1639-87_1639-80del
NM_014714.4:c.3454-87_3454-80del MANE Select NP_055529.2:n.3454-87_3454-80del