Canonical Allele Identifier: CA2545797173

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510473_1510474insT , CM000678.2:g.1510473_1510474insT	GRCh38
NC_000016.9:g.1560474_1560475insT , CM000678.1:g.1560474_1560475insT	GRCh37
NC_000016.8:g.1500475_1500476insT	NCBI36
NG_032783.1:g.106635_106636insA
NG_050910.1:g.22130_22131insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*470_*471insA MANE Select	ENSP00000406012.2:n.*470_*471insA
ENST00000361339.9:c.*470_*471insA	ENSP00000354895.5:n.*470_*471insA
ENST00000397417.6:c.*3297_*3298insA	ENSP00000380562.2:n.*3297_*3298insA
ENST00000426508.6:c.*470_*471insA	ENSP00000406012.2:n.*470_*471insA
ENST00000565298.5:n.4683_4684insA
NM_014714.3:c.*470_*471insA	NP_055529.2:n.*470_*471insA
XM_006720989.2:c.*470_*471insA	XP_006721052.1:n.*470_*471insA
XM_006720990.2:c.*470_*471insA	XP_006721053.1:n.*470_*471insA
XM_006720991.2:c.*470_*471insA	XP_006721054.1:n.*470_*471insA
XM_006720992.2:c.*470_*471insA	XP_006721055.1:n.*470_*471insA
XM_011522766.1:c.*470_*471insA	XP_011521068.1:n.*470_*471insA
XM_011522767.1:c.*470_*471insA	XP_011521069.1:n.*470_*471insA
XM_006720990.3:c.*470_*471insA	XP_006721053.1:n.*470_*471insA
XM_006720991.3:c.*470_*471insA	XP_006721054.1:n.*470_*471insA
XM_006720992.3:c.*470_*471insA	XP_006721055.1:n.*470_*471insA
XM_011522766.3:c.*470_*471insA	XP_011521068.1:n.*470_*471insA
XM_011522767.2:c.*470_*471insA	XP_011521069.1:n.*470_*471insA
XM_017023910.1:c.*470_*471insA	XP_016879399.1:n.*470_*471insA
XM_017023911.1:c.*470_*471insA	XP_016879400.1:n.*470_*471insA
NM_014714.4:c.*470_*471insA MANE Select	NP_055529.2:n.*470_*471insA