Canonical Allele Identifier: CA2805557754

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511103_1511104insACA , CM000678.2:g.1511103_1511104insACA	GRCh38
NC_000016.9:g.1561104_1561105insACA , CM000678.1:g.1561104_1561105insACA	GRCh37
NC_000016.8:g.1501105_1501106insACA	NCBI36
NG_032783.1:g.106005_106006insTGT
NG_050910.1:g.22760_22761insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4229_4230insTGT MANE Select	ENSP00000406012.2:p.Asn1410_Met1411insVal
ENST00000361339.9:c.1811_1812insTGT	ENSP00000354895.5:p.Asn604_Met605insVal
ENST00000397417.6:c.*2667_*2668insTGT	ENSP00000380562.2:n.*2667_*2668insTGT
ENST00000426508.6:c.4229_4230insTGT	ENSP00000406012.2:p.Asn1410_Met1411insVal
ENST00000565298.5:n.4053_4054insTGT
NM_014714.3:c.4229_4230insTGT	NP_055529.2:p.Asn1410_Met1411insVal
XM_006720989.2:c.4229_4230insTGT	XP_006721052.1:p.Asn1410_Met1411insVal
XM_006720990.2:c.4229_4230insTGT	XP_006721053.1:p.Asn1410_Met1411insVal
XM_006720991.2:c.4229_4230insTGT	XP_006721054.1:p.Asn1410_Met1411insVal
XM_006720992.2:c.1862_1863insTGT	XP_006721055.1:p.Asn621_Met622insVal
XM_011522766.1:c.3983_3984insTGT	XP_011521068.1:p.Asn1328_Met1329insVal
XM_011522767.1:c.3254_3255insTGT	XP_011521069.1:p.Asn1085_Met1086insVal
XM_006720990.3:c.4229_4230insTGT	XP_006721053.1:p.Asn1410_Met1411insVal
XM_006720991.3:c.4229_4230insTGT	XP_006721054.1:p.Asn1410_Met1411insVal
XM_006720992.3:c.1862_1863insTGT	XP_006721055.1:p.Asn621_Met622insVal
XM_011522766.3:c.3983_3984insTGT	XP_011521068.1:p.Asn1328_Met1329insVal
XM_011522767.2:c.3254_3255insTGT	XP_011521069.1:p.Asn1085_Met1086insVal
XM_017023910.1:c.4229_4230insTGT	XP_016879399.1:p.Asn1410_Met1411insVal
XM_017023911.1:c.2414_2415insTGT	XP_016879400.1:p.Asn805_Met806insVal
NM_014714.4:c.4229_4230insTGT MANE Select	NP_055529.2:p.Asn1410_Met1411insVal