Canonical Allele Identifier: CA2805557636

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510802_1510803insAT , CM000678.2:g.1510802_1510803insAT	GRCh38
NC_000016.9:g.1560803_1560804insAT , CM000678.1:g.1560803_1560804insAT	GRCh37
NC_000016.8:g.1500804_1500805insAT	NCBI36
NG_032783.1:g.106306_106307insAT
NG_050910.1:g.22459_22460insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*141_*142insAT MANE Select	ENSP00000406012.2:n.*141_*142insAT
ENST00000361339.9:c.*141_*142insAT	ENSP00000354895.5:n.*141_*142insAT
ENST00000397417.6:c.*2968_*2969insAT	ENSP00000380562.2:n.*2968_*2969insAT
ENST00000426508.6:c.*141_*142insAT	ENSP00000406012.2:n.*141_*142insAT
ENST00000565298.5:n.4354_4355insAT
NM_014714.3:c.*141_*142insAT	NP_055529.2:n.*141_*142insAT
XM_006720989.2:c.*141_*142insAT	XP_006721052.1:n.*141_*142insAT
XM_006720990.2:c.*141_*142insAT	XP_006721053.1:n.*141_*142insAT
XM_006720991.2:c.*141_*142insAT	XP_006721054.1:n.*141_*142insAT
XM_006720992.2:c.*141_*142insAT	XP_006721055.1:n.*141_*142insAT
XM_011522766.1:c.*141_*142insAT	XP_011521068.1:n.*141_*142insAT
XM_011522767.1:c.*141_*142insAT	XP_011521069.1:n.*141_*142insAT
XM_006720990.3:c.*141_*142insAT	XP_006721053.1:n.*141_*142insAT
XM_006720991.3:c.*141_*142insAT	XP_006721054.1:n.*141_*142insAT
XM_006720992.3:c.*141_*142insAT	XP_006721055.1:n.*141_*142insAT
XM_011522766.3:c.*141_*142insAT	XP_011521068.1:n.*141_*142insAT
XM_011522767.2:c.*141_*142insAT	XP_011521069.1:n.*141_*142insAT
XM_017023910.1:c.*141_*142insAT	XP_016879399.1:n.*141_*142insAT
XM_017023911.1:c.*141_*142insAT	XP_016879400.1:n.*141_*142insAT
NM_014714.4:c.*141_*142insAT MANE Select	NP_055529.2:n.*141_*142insAT