Canonical Allele Identifier: CA2805557858

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511310_1511311insCC , CM000678.2:g.1511310_1511311insCC	GRCh38
NC_000016.9:g.1561311_1561312insCC , CM000678.1:g.1561311_1561312insCC	GRCh37
NC_000016.8:g.1501312_1501313insCC	NCBI36
NG_032783.1:g.105798_105799insGG
NG_050910.1:g.22967_22968insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-161_4183-160insGG MANE Select	ENSP00000406012.2:n.4183-161_4183-160insGG
ENST00000361339.9:c.1765-161_1765-160insGG	ENSP00000354895.5:n.1765-161_1765-160insGG
ENST00000397417.6:c.*2621-161_*2621-160insGG	ENSP00000380562.2:n.*2621-161_*2621-160insGG
ENST00000426508.6:c.4183-161_4183-160insGG	ENSP00000406012.2:n.4183-161_4183-160insGG
ENST00000565298.5:n.4007-161_4007-160insGG
NM_014714.3:c.4183-161_4183-160insGG	NP_055529.2:n.4183-161_4183-160insGG
XM_006720989.2:c.4183-161_4183-160insGG	XP_006721052.1:n.4183-161_4183-160insGG
XM_006720990.2:c.4183-161_4183-160insGG	XP_006721053.1:n.4183-161_4183-160insGG
XM_006720991.2:c.4183-161_4183-160insGG	XP_006721054.1:n.4183-161_4183-160insGG
XM_006720992.2:c.1816-161_1816-160insGG	XP_006721055.1:n.1816-161_1816-160insGG
XM_011522766.1:c.3937-161_3937-160insGG	XP_011521068.1:n.3937-161_3937-160insGG
XM_011522767.1:c.3208-161_3208-160insGG	XP_011521069.1:n.3208-161_3208-160insGG
XM_006720990.3:c.4183-161_4183-160insGG	XP_006721053.1:n.4183-161_4183-160insGG
XM_006720991.3:c.4183-161_4183-160insGG	XP_006721054.1:n.4183-161_4183-160insGG
XM_006720992.3:c.1816-161_1816-160insGG	XP_006721055.1:n.1816-161_1816-160insGG
XM_011522766.3:c.3937-161_3937-160insGG	XP_011521068.1:n.3937-161_3937-160insGG
XM_011522767.2:c.3208-161_3208-160insGG	XP_011521069.1:n.3208-161_3208-160insGG
XM_017023910.1:c.4183-161_4183-160insGG	XP_016879399.1:n.4183-161_4183-160insGG
XM_017023911.1:c.2368-161_2368-160insGG	XP_016879400.1:n.2368-161_2368-160insGG
NM_014714.4:c.4183-161_4183-160insGG MANE Select	NP_055529.2:n.4183-161_4183-160insGG