Canonical Allele Identifier: CA2805557658

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510863_1510864insTTT , CM000678.2:g.1510863_1510864insTTT	GRCh38
NC_000016.9:g.1560864_1560865insTTT , CM000678.1:g.1560864_1560865insTTT	GRCh37
NC_000016.8:g.1500865_1500866insTTT	NCBI36
NG_032783.1:g.106246_106247insAAA
NG_050910.1:g.22520_22521insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*81_*82insAAA MANE Select	ENSP00000406012.2:n.*81_*82insAAA
ENST00000361339.9:c.*81_*82insAAA	ENSP00000354895.5:n.*81_*82insAAA
ENST00000397417.6:c.*2908_*2909insAAA	ENSP00000380562.2:n.*2908_*2909insAAA
ENST00000426508.6:c.*81_*82insAAA	ENSP00000406012.2:n.*81_*82insAAA
ENST00000565298.5:n.4294_4295insAAA
NM_014714.3:c.*81_*82insAAA	NP_055529.2:n.*81_*82insAAA
XM_006720989.2:c.*81_*82insAAA	XP_006721052.1:n.*81_*82insAAA
XM_006720990.2:c.*81_*82insAAA	XP_006721053.1:n.*81_*82insAAA
XM_006720991.2:c.*81_*82insAAA	XP_006721054.1:n.*81_*82insAAA
XM_006720992.2:c.*81_*82insAAA	XP_006721055.1:n.*81_*82insAAA
XM_011522766.1:c.*81_*82insAAA	XP_011521068.1:n.*81_*82insAAA
XM_011522767.1:c.*81_*82insAAA	XP_011521069.1:n.*81_*82insAAA
XM_006720990.3:c.*81_*82insAAA	XP_006721053.1:n.*81_*82insAAA
XM_006720991.3:c.*81_*82insAAA	XP_006721054.1:n.*81_*82insAAA
XM_006720992.3:c.*81_*82insAAA	XP_006721055.1:n.*81_*82insAAA
XM_011522766.3:c.*81_*82insAAA	XP_011521068.1:n.*81_*82insAAA
XM_011522767.2:c.*81_*82insAAA	XP_011521069.1:n.*81_*82insAAA
XM_017023910.1:c.*81_*82insAAA	XP_016879399.1:n.*81_*82insAAA
XM_017023911.1:c.*81_*82insAAA	XP_016879400.1:n.*81_*82insAAA
NM_014714.4:c.*81_*82insAAA MANE Select	NP_055529.2:n.*81_*82insAAA