Canonical Allele Identifier: CA7812846
Gene: IFT140 HGNC NCBI

Linked Data

dbSNP Id: rs3833844

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1511190_1511214del , CM000678.2:g.1511190_1511214del GRCh38
NC_000016.9:g.1561191_1561215del , CM000678.1:g.1561191_1561215del GRCh37
NC_000016.8:g.1501192_1501216del NCBI36
NG_032783.1:g.105895_105919del
NG_050910.1:g.22847_22871del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.4183-64_4183-40del MANE Select ENSP00000406012.2:n.4183-64_4183-40del
ENST00000361339.9:c.1765-64_1765-40del ENSP00000354895.5:n.1765-64_1765-40del
ENST00000397417.6:c.*2621-64_*2621-40del ENSP00000380562.2:n.*2621-64_*2621-40del
ENST00000426508.6:c.4183-64_4183-40del ENSP00000406012.2:n.4183-64_4183-40del
ENST00000565298.5:n.4007-64_4007-40del
NM_014714.3:c.4183-64_4183-40del NP_055529.2:n.4183-64_4183-40del
XM_006720989.2:c.4183-64_4183-40del XP_006721052.1:n.4183-64_4183-40del
XM_006720990.2:c.4183-64_4183-40del XP_006721053.1:n.4183-64_4183-40del
XM_006720991.2:c.4183-64_4183-40del XP_006721054.1:n.4183-64_4183-40del
XM_006720992.2:c.1816-64_1816-40del XP_006721055.1:n.1816-64_1816-40del
XM_011522766.1:c.3937-64_3937-40del XP_011521068.1:n.3937-64_3937-40del
XM_011522767.1:c.3208-64_3208-40del XP_011521069.1:n.3208-64_3208-40del
XM_006720990.3:c.4183-64_4183-40del XP_006721053.1:n.4183-64_4183-40del
XM_006720991.3:c.4183-64_4183-40del XP_006721054.1:n.4183-64_4183-40del
XM_006720992.3:c.1816-64_1816-40del XP_006721055.1:n.1816-64_1816-40del
XM_011522766.3:c.3937-64_3937-40del XP_011521068.1:n.3937-64_3937-40del
XM_011522767.2:c.3208-64_3208-40del XP_011521069.1:n.3208-64_3208-40del
XM_017023910.1:c.4183-64_4183-40del XP_016879399.1:n.4183-64_4183-40del
XM_017023911.1:c.2368-64_2368-40del XP_016879400.1:n.2368-64_2368-40del
NM_014714.4:c.4183-64_4183-40del MANE Select NP_055529.2:n.4183-64_4183-40del