Canonical Allele Identifier: CA718376414
Gene: IFT140 HGNC NCBI

Linked Data

dbSNP Id: rs1309157857

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1511302dup , CM000678.2:g.1511302dup GRCh38
NC_000016.9:g.1561303dup , CM000678.1:g.1561303dup GRCh37
NC_000016.8:g.1501304dup NCBI36
NG_032783.1:g.105807dup
NG_050910.1:g.22959dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000426508.7:c.4183-152dup MANE Select ENSP00000406012.2:n.4183-152dup
ENST00000361339.9:c.1765-152dup ENSP00000354895.5:n.1765-152dup
ENST00000397417.6:c.*2621-152dup ENSP00000380562.2:n.*2621-152dup
ENST00000426508.6:c.4183-152dup ENSP00000406012.2:n.4183-152dup
ENST00000565298.5:n.4007-152dup
NM_014714.3:c.4183-152dup NP_055529.2:n.4183-152dup
XM_006720989.2:c.4183-152dup XP_006721052.1:n.4183-152dup
XM_006720990.2:c.4183-152dup XP_006721053.1:n.4183-152dup
XM_006720991.2:c.4183-152dup XP_006721054.1:n.4183-152dup
XM_006720992.2:c.1816-152dup XP_006721055.1:n.1816-152dup
XM_011522766.1:c.3937-152dup XP_011521068.1:n.3937-152dup
XM_011522767.1:c.3208-152dup XP_011521069.1:n.3208-152dup
XM_006720990.3:c.4183-152dup XP_006721053.1:n.4183-152dup
XM_006720991.3:c.4183-152dup XP_006721054.1:n.4183-152dup
XM_006720992.3:c.1816-152dup XP_006721055.1:n.1816-152dup
XM_011522766.3:c.3937-152dup XP_011521068.1:n.3937-152dup
XM_011522767.2:c.3208-152dup XP_011521069.1:n.3208-152dup
XM_017023910.1:c.4183-152dup XP_016879399.1:n.4183-152dup
XM_017023911.1:c.2368-152dup XP_016879400.1:n.2368-152dup
NM_014714.4:c.4183-152dup MANE Select NP_055529.2:n.4183-152dup