Canonical Allele Identifier: CA2631007402

Gene: IFT140

Linked Data

• gnomAD v4: 16-1511244-C-CACCCCCACCCGCCTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511244_1511245insACCCCCACCCGCCTCCA , CM000678.2:g.1511244_1511245insACCCCCACCCGCCTCCA	GRCh38
NC_000016.9:g.1561245_1561246insACCCCCACCCGCCTCCA , CM000678.1:g.1561245_1561246insACCCCCACCCGCCTCCA	GRCh37
NC_000016.8:g.1501246_1501247insACCCCCACCCGCCTCCA	NCBI36
NG_032783.1:g.105864_105865insTGGAGGCGGGTGGGGGT
NG_050910.1:g.22901_22902insACCCCCACCCGCCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT MANE Select	ENSP00000406012.2:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
ENST00000361339.9:c.1765-95_1765-94insTGGAGGCGGGTGGGGGT	ENSP00000354895.5:n.1765-95_1765-94insTGGAGGCGGGTGGGGGT
ENST00000397417.6:c.*2621-95_*2621-94insTGGAGGCGGGTGGGGGT	ENSP00000380562.2:n.*2621-95_*2621-94insTGGAGGCGGGTGGGGGT
ENST00000426508.6:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	ENSP00000406012.2:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
ENST00000565298.5:n.4007-95_4007-94insTGGAGGCGGGTGGGGGT
NM_014714.3:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	NP_055529.2:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720989.2:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_006721052.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720990.2:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_006721053.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720991.2:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_006721054.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720992.2:c.1816-95_1816-94insTGGAGGCGGGTGGGGGT	XP_006721055.1:n.1816-95_1816-94insTGGAGGCGGGTGGGGGT
XM_011522766.1:c.3937-95_3937-94insTGGAGGCGGGTGGGGGT	XP_011521068.1:n.3937-95_3937-94insTGGAGGCGGGTGGGGGT
XM_011522767.1:c.3208-95_3208-94insTGGAGGCGGGTGGGGGT	XP_011521069.1:n.3208-95_3208-94insTGGAGGCGGGTGGGGGT
XM_006720990.3:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_006721053.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720991.3:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_006721054.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_006720992.3:c.1816-95_1816-94insTGGAGGCGGGTGGGGGT	XP_006721055.1:n.1816-95_1816-94insTGGAGGCGGGTGGGGGT
XM_011522766.3:c.3937-95_3937-94insTGGAGGCGGGTGGGGGT	XP_011521068.1:n.3937-95_3937-94insTGGAGGCGGGTGGGGGT
XM_011522767.2:c.3208-95_3208-94insTGGAGGCGGGTGGGGGT	XP_011521069.1:n.3208-95_3208-94insTGGAGGCGGGTGGGGGT
XM_017023910.1:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT	XP_016879399.1:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT
XM_017023911.1:c.2368-95_2368-94insTGGAGGCGGGTGGGGGT	XP_016879400.1:n.2368-95_2368-94insTGGAGGCGGGTGGGGGT
NM_014714.4:c.4183-95_4183-94insTGGAGGCGGGTGGGGGT MANE Select	NP_055529.2:n.4183-95_4183-94insTGGAGGCGGGTGGGGGT