Canonical Allele Identifier: CA2805558989

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520869_1520870insA , CM000678.2:g.1520869_1520870insA	GRCh38
NC_000016.9:g.1570870_1570871insA , CM000678.1:g.1570870_1570871insA	GRCh37
NC_000016.8:g.1510871_1510872insA	NCBI36
NG_032783.1:g.96239_96240insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3454-62_3454-61insT MANE Select	ENSP00000406012.2:n.3454-62_3454-61insT
ENST00000361339.9:c.1036-62_1036-61insT	ENSP00000354895.5:n.1036-62_1036-61insT
ENST00000397417.6:c.*1892-62_*1892-61insT	ENSP00000380562.2:n.*1892-62_*1892-61insT
ENST00000426508.6:c.3454-62_3454-61insT	ENSP00000406012.2:n.3454-62_3454-61insT
ENST00000565298.5:n.3278-62_3278-61insT
NM_014714.3:c.3454-62_3454-61insT	NP_055529.2:n.3454-62_3454-61insT
XM_006720989.2:c.3454-62_3454-61insT	XP_006721052.1:n.3454-62_3454-61insT
XM_006720990.2:c.3454-62_3454-61insT	XP_006721053.1:n.3454-62_3454-61insT
XM_006720991.2:c.3454-62_3454-61insT	XP_006721054.1:n.3454-62_3454-61insT
XM_006720992.2:c.1087-62_1087-61insT	XP_006721055.1:n.1087-62_1087-61insT
XM_011522766.1:c.3208-62_3208-61insT	XP_011521068.1:n.3208-62_3208-61insT
XM_011522767.1:c.2479-62_2479-61insT	XP_011521069.1:n.2479-62_2479-61insT
XM_006720990.3:c.3454-62_3454-61insT	XP_006721053.1:n.3454-62_3454-61insT
XM_006720991.3:c.3454-62_3454-61insT	XP_006721054.1:n.3454-62_3454-61insT
XM_006720992.3:c.1087-62_1087-61insT	XP_006721055.1:n.1087-62_1087-61insT
XM_011522766.3:c.3208-62_3208-61insT	XP_011521068.1:n.3208-62_3208-61insT
XM_011522767.2:c.2479-62_2479-61insT	XP_011521069.1:n.2479-62_2479-61insT
XM_017023910.1:c.3454-62_3454-61insT	XP_016879399.1:n.3454-62_3454-61insT
XM_017023911.1:c.1639-62_1639-61insT	XP_016879400.1:n.1639-62_1639-61insT
NM_014714.4:c.3454-62_3454-61insT MANE Select	NP_055529.2:n.3454-62_3454-61insT