Canonical Allele Identifier: CA2805557842

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511297_1511298insA , CM000678.2:g.1511297_1511298insA	GRCh38
NC_000016.9:g.1561298_1561299insA , CM000678.1:g.1561298_1561299insA	GRCh37
NC_000016.8:g.1501299_1501300insA	NCBI36
NG_032783.1:g.105811_105812insT
NG_050910.1:g.22954_22955insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-148_4183-147insT MANE Select	ENSP00000406012.2:n.4183-148_4183-147insT
ENST00000361339.9:c.1765-148_1765-147insT	ENSP00000354895.5:n.1765-148_1765-147insT
ENST00000397417.6:c.*2621-148_*2621-147insT	ENSP00000380562.2:n.*2621-148_*2621-147insT
ENST00000426508.6:c.4183-148_4183-147insT	ENSP00000406012.2:n.4183-148_4183-147insT
ENST00000565298.5:n.4007-148_4007-147insT
NM_014714.3:c.4183-148_4183-147insT	NP_055529.2:n.4183-148_4183-147insT
XM_006720989.2:c.4183-148_4183-147insT	XP_006721052.1:n.4183-148_4183-147insT
XM_006720990.2:c.4183-148_4183-147insT	XP_006721053.1:n.4183-148_4183-147insT
XM_006720991.2:c.4183-148_4183-147insT	XP_006721054.1:n.4183-148_4183-147insT
XM_006720992.2:c.1816-148_1816-147insT	XP_006721055.1:n.1816-148_1816-147insT
XM_011522766.1:c.3937-148_3937-147insT	XP_011521068.1:n.3937-148_3937-147insT
XM_011522767.1:c.3208-148_3208-147insT	XP_011521069.1:n.3208-148_3208-147insT
XM_006720990.3:c.4183-148_4183-147insT	XP_006721053.1:n.4183-148_4183-147insT
XM_006720991.3:c.4183-148_4183-147insT	XP_006721054.1:n.4183-148_4183-147insT
XM_006720992.3:c.1816-148_1816-147insT	XP_006721055.1:n.1816-148_1816-147insT
XM_011522766.3:c.3937-148_3937-147insT	XP_011521068.1:n.3937-148_3937-147insT
XM_011522767.2:c.3208-148_3208-147insT	XP_011521069.1:n.3208-148_3208-147insT
XM_017023910.1:c.4183-148_4183-147insT	XP_016879399.1:n.4183-148_4183-147insT
XM_017023911.1:c.2368-148_2368-147insT	XP_016879400.1:n.2368-148_2368-147insT
NM_014714.4:c.4183-148_4183-147insT MANE Select	NP_055529.2:n.4183-148_4183-147insT