Canonical Allele Identifier: CA2805557755

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511121_1511122insA , CM000678.2:g.1511121_1511122insA	GRCh38
NC_000016.9:g.1561122_1561123insA , CM000678.1:g.1561122_1561123insA	GRCh37
NC_000016.8:g.1501123_1501124insA	NCBI36
NG_032783.1:g.105987_105988insT
NG_050910.1:g.22778_22779insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4211_4212insT MANE Select	ENSP00000406012.2:p.Arg1405AlafsTer?
ENST00000361339.9:c.1793_1794insT	ENSP00000354895.5:p.Arg599AlafsTer?
ENST00000397417.6:c.*2649_*2650insT	ENSP00000380562.2:n.*2649_*2650insT
ENST00000426508.6:c.4211_4212insT	ENSP00000406012.2:p.Arg1405AlafsTer?
ENST00000565298.5:n.4035_4036insT
NM_014714.3:c.4211_4212insT	NP_055529.2:p.Arg1405AlafsTer?
XM_006720989.2:c.4211_4212insT	XP_006721052.1:p.Arg1405AlafsTer?
XM_006720990.2:c.4211_4212insT	XP_006721053.1:p.Arg1405AlafsTer?
XM_006720991.2:c.4211_4212insT	XP_006721054.1:p.Arg1405AlafsTer?
XM_006720992.2:c.1844_1845insT	XP_006721055.1:p.Arg616AlafsTer?
XM_011522766.1:c.3965_3966insT	XP_011521068.1:p.Arg1323AlafsTer?
XM_011522767.1:c.3236_3237insT	XP_011521069.1:p.Arg1080AlafsTer?
XM_006720990.3:c.4211_4212insT	XP_006721053.1:p.Arg1405AlafsTer?
XM_006720991.3:c.4211_4212insT	XP_006721054.1:p.Arg1405AlafsTer?
XM_006720992.3:c.1844_1845insT	XP_006721055.1:p.Arg616AlafsTer?
XM_011522766.3:c.3965_3966insT	XP_011521068.1:p.Arg1323AlafsTer?
XM_011522767.2:c.3236_3237insT	XP_011521069.1:p.Arg1080AlafsTer?
XM_017023910.1:c.4211_4212insT	XP_016879399.1:p.Arg1405AlafsTer?
XM_017023911.1:c.2396_2397insT	XP_016879400.1:p.Arg800AlafsTer?
NM_014714.4:c.4211_4212insT MANE Select	NP_055529.2:p.Arg1405AlafsTer?