Canonical Allele Identifier: CA2805557825

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511275_1511276insAC , CM000678.2:g.1511275_1511276insAC	GRCh38
NC_000016.9:g.1561276_1561277insAC , CM000678.1:g.1561276_1561277insAC	GRCh37
NC_000016.8:g.1501277_1501278insAC	NCBI36
NG_032783.1:g.105833_105834insGT
NG_050910.1:g.22932_22933insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-126_4183-125insGT MANE Select	ENSP00000406012.2:n.4183-126_4183-125insGT
ENST00000361339.9:c.1765-126_1765-125insGT	ENSP00000354895.5:n.1765-126_1765-125insGT
ENST00000397417.6:c.*2621-126_*2621-125insGT	ENSP00000380562.2:n.*2621-126_*2621-125insGT
ENST00000426508.6:c.4183-126_4183-125insGT	ENSP00000406012.2:n.4183-126_4183-125insGT
ENST00000565298.5:n.4007-126_4007-125insGT
NM_014714.3:c.4183-126_4183-125insGT	NP_055529.2:n.4183-126_4183-125insGT
XM_006720989.2:c.4183-126_4183-125insGT	XP_006721052.1:n.4183-126_4183-125insGT
XM_006720990.2:c.4183-126_4183-125insGT	XP_006721053.1:n.4183-126_4183-125insGT
XM_006720991.2:c.4183-126_4183-125insGT	XP_006721054.1:n.4183-126_4183-125insGT
XM_006720992.2:c.1816-126_1816-125insGT	XP_006721055.1:n.1816-126_1816-125insGT
XM_011522766.1:c.3937-126_3937-125insGT	XP_011521068.1:n.3937-126_3937-125insGT
XM_011522767.1:c.3208-126_3208-125insGT	XP_011521069.1:n.3208-126_3208-125insGT
XM_006720990.3:c.4183-126_4183-125insGT	XP_006721053.1:n.4183-126_4183-125insGT
XM_006720991.3:c.4183-126_4183-125insGT	XP_006721054.1:n.4183-126_4183-125insGT
XM_006720992.3:c.1816-126_1816-125insGT	XP_006721055.1:n.1816-126_1816-125insGT
XM_011522766.3:c.3937-126_3937-125insGT	XP_011521068.1:n.3937-126_3937-125insGT
XM_011522767.2:c.3208-126_3208-125insGT	XP_011521069.1:n.3208-126_3208-125insGT
XM_017023910.1:c.4183-126_4183-125insGT	XP_016879399.1:n.4183-126_4183-125insGT
XM_017023911.1:c.2368-126_2368-125insGT	XP_016879400.1:n.2368-126_2368-125insGT
NM_014714.4:c.4183-126_4183-125insGT MANE Select	NP_055529.2:n.4183-126_4183-125insGT