Canonical Allele Identifier: CA2201718254

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510817_1510819delinsGCT , CM000678.2:g.1510817_1510819delinsGCT	GRCh38
NC_000016.9:g.1560818_1560820delinsGCT , CM000678.1:g.1560818_1560820delinsGCT	GRCh37
NC_000016.8:g.1500819_1500821delinsGCT	NCBI36
NG_032783.1:g.106290_106292delinsAGC
NG_050910.1:g.22474_22476delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*125_*127delinsAGC MANE Select	ENSP00000406012.2:n.*125_*127delinsAGC
ENST00000361339.9:c.*125_*127delinsAGC	ENSP00000354895.5:n.*125_*127delinsAGC
ENST00000397417.6:c.*2952_*2954delinsAGC	ENSP00000380562.2:n.*2952_*2954delinsAGC
ENST00000426508.6:c.*125_*127delinsAGC	ENSP00000406012.2:n.*125_*127delinsAGC
ENST00000565298.5:n.4338_4340delinsAGC
NM_014714.3:c.*125_*127delinsAGC	NP_055529.2:n.*125_*127delinsAGC
XM_006720989.2:c.*125_*127delinsAGC	XP_006721052.1:n.*125_*127delinsAGC
XM_006720990.2:c.*125_*127delinsAGC	XP_006721053.1:n.*125_*127delinsAGC
XM_006720991.2:c.*125_*127delinsAGC	XP_006721054.1:n.*125_*127delinsAGC
XM_006720992.2:c.*125_*127delinsAGC	XP_006721055.1:n.*125_*127delinsAGC
XM_011522766.1:c.*125_*127delinsAGC	XP_011521068.1:n.*125_*127delinsAGC
XM_011522767.1:c.*125_*127delinsAGC	XP_011521069.1:n.*125_*127delinsAGC
XM_006720990.3:c.*125_*127delinsAGC	XP_006721053.1:n.*125_*127delinsAGC
XM_006720991.3:c.*125_*127delinsAGC	XP_006721054.1:n.*125_*127delinsAGC
XM_006720992.3:c.*125_*127delinsAGC	XP_006721055.1:n.*125_*127delinsAGC
XM_011522766.3:c.*125_*127delinsAGC	XP_011521068.1:n.*125_*127delinsAGC
XM_011522767.2:c.*125_*127delinsAGC	XP_011521069.1:n.*125_*127delinsAGC
XM_017023910.1:c.*125_*127delinsAGC	XP_016879399.1:n.*125_*127delinsAGC
XM_017023911.1:c.*125_*127delinsAGC	XP_016879400.1:n.*125_*127delinsAGC
NM_014714.4:c.*125_*127delinsAGC MANE Select	NP_055529.2:n.*125_*127delinsAGC