Canonical Allele Identifier: CA2805557764

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511207_1511208insACG , CM000678.2:g.1511207_1511208insACG	GRCh38
NC_000016.9:g.1561208_1561209insACG , CM000678.1:g.1561208_1561209insACG	GRCh37
NC_000016.8:g.1501209_1501210insACG	NCBI36
NG_032783.1:g.105901_105902insCGT
NG_050910.1:g.22864_22865insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-58_4183-57insCGT MANE Select	ENSP00000406012.2:n.4183-58_4183-57insCGT
ENST00000361339.9:c.1765-58_1765-57insCGT	ENSP00000354895.5:n.1765-58_1765-57insCGT
ENST00000397417.6:c.*2621-58_*2621-57insCGT	ENSP00000380562.2:n.*2621-58_*2621-57insCGT
ENST00000426508.6:c.4183-58_4183-57insCGT	ENSP00000406012.2:n.4183-58_4183-57insCGT
ENST00000565298.5:n.4007-58_4007-57insCGT
NM_014714.3:c.4183-58_4183-57insCGT	NP_055529.2:n.4183-58_4183-57insCGT
XM_006720989.2:c.4183-58_4183-57insCGT	XP_006721052.1:n.4183-58_4183-57insCGT
XM_006720990.2:c.4183-58_4183-57insCGT	XP_006721053.1:n.4183-58_4183-57insCGT
XM_006720991.2:c.4183-58_4183-57insCGT	XP_006721054.1:n.4183-58_4183-57insCGT
XM_006720992.2:c.1816-58_1816-57insCGT	XP_006721055.1:n.1816-58_1816-57insCGT
XM_011522766.1:c.3937-58_3937-57insCGT	XP_011521068.1:n.3937-58_3937-57insCGT
XM_011522767.1:c.3208-58_3208-57insCGT	XP_011521069.1:n.3208-58_3208-57insCGT
XM_006720990.3:c.4183-58_4183-57insCGT	XP_006721053.1:n.4183-58_4183-57insCGT
XM_006720991.3:c.4183-58_4183-57insCGT	XP_006721054.1:n.4183-58_4183-57insCGT
XM_006720992.3:c.1816-58_1816-57insCGT	XP_006721055.1:n.1816-58_1816-57insCGT
XM_011522766.3:c.3937-58_3937-57insCGT	XP_011521068.1:n.3937-58_3937-57insCGT
XM_011522767.2:c.3208-58_3208-57insCGT	XP_011521069.1:n.3208-58_3208-57insCGT
XM_017023910.1:c.4183-58_4183-57insCGT	XP_016879399.1:n.4183-58_4183-57insCGT
XM_017023911.1:c.2368-58_2368-57insCGT	XP_016879400.1:n.2368-58_2368-57insCGT
NM_014714.4:c.4183-58_4183-57insCGT MANE Select	NP_055529.2:n.4183-58_4183-57insCGT