Canonical Allele Identifier: CA2805558988

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520855_1520856insCAC , CM000678.2:g.1520855_1520856insCAC	GRCh38
NC_000016.9:g.1570856_1570857insCAC , CM000678.1:g.1570856_1570857insCAC	GRCh37
NC_000016.8:g.1510857_1510858insCAC	NCBI36
NG_032783.1:g.96255_96256insGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3454-46_3454-45insGGT MANE Select	ENSP00000406012.2:n.3454-46_3454-45insGGT
ENST00000361339.9:c.1036-46_1036-45insGGT	ENSP00000354895.5:n.1036-46_1036-45insGGT
ENST00000397417.6:c.*1892-46_*1892-45insGGT	ENSP00000380562.2:n.*1892-46_*1892-45insGGT
ENST00000426508.6:c.3454-46_3454-45insGGT	ENSP00000406012.2:n.3454-46_3454-45insGGT
ENST00000565298.5:n.3278-46_3278-45insGGT
NM_014714.3:c.3454-46_3454-45insGGT	NP_055529.2:n.3454-46_3454-45insGGT
XM_006720989.2:c.3454-46_3454-45insGGT	XP_006721052.1:n.3454-46_3454-45insGGT
XM_006720990.2:c.3454-46_3454-45insGGT	XP_006721053.1:n.3454-46_3454-45insGGT
XM_006720991.2:c.3454-46_3454-45insGGT	XP_006721054.1:n.3454-46_3454-45insGGT
XM_006720992.2:c.1087-46_1087-45insGGT	XP_006721055.1:n.1087-46_1087-45insGGT
XM_011522766.1:c.3208-46_3208-45insGGT	XP_011521068.1:n.3208-46_3208-45insGGT
XM_011522767.1:c.2479-46_2479-45insGGT	XP_011521069.1:n.2479-46_2479-45insGGT
XM_006720990.3:c.3454-46_3454-45insGGT	XP_006721053.1:n.3454-46_3454-45insGGT
XM_006720991.3:c.3454-46_3454-45insGGT	XP_006721054.1:n.3454-46_3454-45insGGT
XM_006720992.3:c.1087-46_1087-45insGGT	XP_006721055.1:n.1087-46_1087-45insGGT
XM_011522766.3:c.3208-46_3208-45insGGT	XP_011521068.1:n.3208-46_3208-45insGGT
XM_011522767.2:c.2479-46_2479-45insGGT	XP_011521069.1:n.2479-46_2479-45insGGT
XM_017023910.1:c.3454-46_3454-45insGGT	XP_016879399.1:n.3454-46_3454-45insGGT
XM_017023911.1:c.1639-46_1639-45insGGT	XP_016879400.1:n.1639-46_1639-45insGGT
NM_014714.4:c.3454-46_3454-45insGGT MANE Select	NP_055529.2:n.3454-46_3454-45insGGT