Canonical Allele Identifier: CA2526464403

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1510498_1510499insTAAAAAAT , CM000678.2:g.1510498_1510499insTAAAAAAT	GRCh38
NC_000016.9:g.1560499_1560500insTAAAAAAT , CM000678.1:g.1560499_1560500insTAAAAAAT	GRCh37
NC_000016.8:g.1500500_1500501insTAAAAAAT	NCBI36
NG_032783.1:g.106611_106612insTTTTTTAA
NG_050910.1:g.22155_22156insTAAAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.*446_*447insTTTTTTAA MANE Select	ENSP00000406012.2:n.*446_*447insTTTTTTAA
ENST00000361339.9:c.*446_*447insTTTTTTAA	ENSP00000354895.5:n.*446_*447insTTTTTTAA
ENST00000397417.6:c.*3273_*3274insTTTTTTAA	ENSP00000380562.2:n.*3273_*3274insTTTTTTAA
ENST00000426508.6:c.*446_*447insTTTTTTAA	ENSP00000406012.2:n.*446_*447insTTTTTTAA
ENST00000565298.5:n.4659_4660insTTTTTTAA
NM_014714.3:c.*446_*447insTTTTTTAA	NP_055529.2:n.*446_*447insTTTTTTAA
XM_006720989.2:c.*446_*447insTTTTTTAA	XP_006721052.1:n.*446_*447insTTTTTTAA
XM_006720990.2:c.*446_*447insTTTTTTAA	XP_006721053.1:n.*446_*447insTTTTTTAA
XM_006720991.2:c.*446_*447insTTTTTTAA	XP_006721054.1:n.*446_*447insTTTTTTAA
XM_006720992.2:c.*446_*447insTTTTTTAA	XP_006721055.1:n.*446_*447insTTTTTTAA
XM_011522766.1:c.*446_*447insTTTTTTAA	XP_011521068.1:n.*446_*447insTTTTTTAA
XM_011522767.1:c.*446_*447insTTTTTTAA	XP_011521069.1:n.*446_*447insTTTTTTAA
XM_006720990.3:c.*446_*447insTTTTTTAA	XP_006721053.1:n.*446_*447insTTTTTTAA
XM_006720991.3:c.*446_*447insTTTTTTAA	XP_006721054.1:n.*446_*447insTTTTTTAA
XM_006720992.3:c.*446_*447insTTTTTTAA	XP_006721055.1:n.*446_*447insTTTTTTAA
XM_011522766.3:c.*446_*447insTTTTTTAA	XP_011521068.1:n.*446_*447insTTTTTTAA
XM_011522767.2:c.*446_*447insTTTTTTAA	XP_011521069.1:n.*446_*447insTTTTTTAA
XM_017023910.1:c.*446_*447insTTTTTTAA	XP_016879399.1:n.*446_*447insTTTTTTAA
XM_017023911.1:c.*446_*447insTTTTTTAA	XP_016879400.1:n.*446_*447insTTTTTTAA
NM_014714.4:c.*446_*447insTTTTTTAA MANE Select	NP_055529.2:n.*446_*447insTTTTTTAA