Canonical Allele Identifier: CA2805557772

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511232_1511233insA , CM000678.2:g.1511232_1511233insA	GRCh38
NC_000016.9:g.1561233_1561234insA , CM000678.1:g.1561233_1561234insA	GRCh37
NC_000016.8:g.1501234_1501235insA	NCBI36
NG_032783.1:g.105876_105877insT
NG_050910.1:g.22889_22890insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-83_4183-82insT MANE Select	ENSP00000406012.2:n.4183-83_4183-82insT
ENST00000361339.9:c.1765-83_1765-82insT	ENSP00000354895.5:n.1765-83_1765-82insT
ENST00000397417.6:c.*2621-83_*2621-82insT	ENSP00000380562.2:n.*2621-83_*2621-82insT
ENST00000426508.6:c.4183-83_4183-82insT	ENSP00000406012.2:n.4183-83_4183-82insT
ENST00000565298.5:n.4007-83_4007-82insT
NM_014714.3:c.4183-83_4183-82insT	NP_055529.2:n.4183-83_4183-82insT
XM_006720989.2:c.4183-83_4183-82insT	XP_006721052.1:n.4183-83_4183-82insT
XM_006720990.2:c.4183-83_4183-82insT	XP_006721053.1:n.4183-83_4183-82insT
XM_006720991.2:c.4183-83_4183-82insT	XP_006721054.1:n.4183-83_4183-82insT
XM_006720992.2:c.1816-83_1816-82insT	XP_006721055.1:n.1816-83_1816-82insT
XM_011522766.1:c.3937-83_3937-82insT	XP_011521068.1:n.3937-83_3937-82insT
XM_011522767.1:c.3208-83_3208-82insT	XP_011521069.1:n.3208-83_3208-82insT
XM_006720990.3:c.4183-83_4183-82insT	XP_006721053.1:n.4183-83_4183-82insT
XM_006720991.3:c.4183-83_4183-82insT	XP_006721054.1:n.4183-83_4183-82insT
XM_006720992.3:c.1816-83_1816-82insT	XP_006721055.1:n.1816-83_1816-82insT
XM_011522766.3:c.3937-83_3937-82insT	XP_011521068.1:n.3937-83_3937-82insT
XM_011522767.2:c.3208-83_3208-82insT	XP_011521069.1:n.3208-83_3208-82insT
XM_017023910.1:c.4183-83_4183-82insT	XP_016879399.1:n.4183-83_4183-82insT
XM_017023911.1:c.2368-83_2368-82insT	XP_016879400.1:n.2368-83_2368-82insT
NM_014714.4:c.4183-83_4183-82insT MANE Select	NP_055529.2:n.4183-83_4183-82insT