Canonical Allele Identifier: CA2805557766

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1511217_1511218del , CM000678.2:g.1511217_1511218del	GRCh38
NC_000016.9:g.1561218_1561219del , CM000678.1:g.1561218_1561219del	GRCh37
NC_000016.8:g.1501219_1501220del	NCBI36
NG_032783.1:g.105891_105892del
NG_050910.1:g.22874_22875del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.4183-68_4183-67del MANE Select	ENSP00000406012.2:n.4183-68_4183-67del
ENST00000361339.9:c.1765-68_1765-67del	ENSP00000354895.5:n.1765-68_1765-67del
ENST00000397417.6:c.*2621-68_*2621-67del	ENSP00000380562.2:n.*2621-68_*2621-67del
ENST00000426508.6:c.4183-68_4183-67del	ENSP00000406012.2:n.4183-68_4183-67del
ENST00000565298.5:n.4007-68_4007-67del
NM_014714.3:c.4183-68_4183-67del	NP_055529.2:n.4183-68_4183-67del
XM_006720989.2:c.4183-68_4183-67del	XP_006721052.1:n.4183-68_4183-67del
XM_006720990.2:c.4183-68_4183-67del	XP_006721053.1:n.4183-68_4183-67del
XM_006720991.2:c.4183-68_4183-67del	XP_006721054.1:n.4183-68_4183-67del
XM_006720992.2:c.1816-68_1816-67del	XP_006721055.1:n.1816-68_1816-67del
XM_011522766.1:c.3937-68_3937-67del	XP_011521068.1:n.3937-68_3937-67del
XM_011522767.1:c.3208-68_3208-67del	XP_011521069.1:n.3208-68_3208-67del
XM_006720990.3:c.4183-68_4183-67del	XP_006721053.1:n.4183-68_4183-67del
XM_006720991.3:c.4183-68_4183-67del	XP_006721054.1:n.4183-68_4183-67del
XM_006720992.3:c.1816-68_1816-67del	XP_006721055.1:n.1816-68_1816-67del
XM_011522766.3:c.3937-68_3937-67del	XP_011521068.1:n.3937-68_3937-67del
XM_011522767.2:c.3208-68_3208-67del	XP_011521069.1:n.3208-68_3208-67del
XM_017023910.1:c.4183-68_4183-67del	XP_016879399.1:n.4183-68_4183-67del
XM_017023911.1:c.2368-68_2368-67del	XP_016879400.1:n.2368-68_2368-67del
NM_014714.4:c.4183-68_4183-67del MANE Select	NP_055529.2:n.4183-68_4183-67del