Canonical Allele Identifier: CA2201718087

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510477_1510478delinsTG , CM000678.2:g.1510477_1510478delinsTG	GRCh38
NC_000016.9:g.1560478_1560479delinsTG , CM000678.1:g.1560478_1560479delinsTG	GRCh37
NC_000016.8:g.1500479_1500480delinsTG	NCBI36
NG_032783.1:g.106631_106632delinsCA
NG_050910.1:g.22134_22135delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*466_*467delinsCA MANE Select	ENSP00000406012.2:n.*466_*467delinsCA
ENST00000361339.9:c.*466_*467delinsCA	ENSP00000354895.5:n.*466_*467delinsCA
ENST00000397417.6:c.*3293_*3294delinsCA	ENSP00000380562.2:n.*3293_*3294delinsCA
ENST00000426508.6:c.*466_*467delinsCA	ENSP00000406012.2:n.*466_*467delinsCA
ENST00000565298.5:n.4679_4680delinsCA
NM_014714.3:c.*466_*467delinsCA	NP_055529.2:n.*466_*467delinsCA
XM_006720989.2:c.*466_*467delinsCA	XP_006721052.1:n.*466_*467delinsCA
XM_006720990.2:c.*466_*467delinsCA	XP_006721053.1:n.*466_*467delinsCA
XM_006720991.2:c.*466_*467delinsCA	XP_006721054.1:n.*466_*467delinsCA
XM_006720992.2:c.*466_*467delinsCA	XP_006721055.1:n.*466_*467delinsCA
XM_011522766.1:c.*466_*467delinsCA	XP_011521068.1:n.*466_*467delinsCA
XM_011522767.1:c.*466_*467delinsCA	XP_011521069.1:n.*466_*467delinsCA
XM_006720990.3:c.*466_*467delinsCA	XP_006721053.1:n.*466_*467delinsCA
XM_006720991.3:c.*466_*467delinsCA	XP_006721054.1:n.*466_*467delinsCA
XM_006720992.3:c.*466_*467delinsCA	XP_006721055.1:n.*466_*467delinsCA
XM_011522766.3:c.*466_*467delinsCA	XP_011521068.1:n.*466_*467delinsCA
XM_011522767.2:c.*466_*467delinsCA	XP_011521069.1:n.*466_*467delinsCA
XM_017023910.1:c.*466_*467delinsCA	XP_016879399.1:n.*466_*467delinsCA
XM_017023911.1:c.*466_*467delinsCA	XP_016879400.1:n.*466_*467delinsCA
NM_014714.4:c.*466_*467delinsCA MANE Select	NP_055529.2:n.*466_*467delinsCA