Canonical Allele Identifier: CA2631008563

Gene: IFT140

Linked Data

• gnomAD v4: 16-1525874-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525874G>T , CM000678.2:g.1525874G>T	GRCh38
NC_000016.9:g.1575875G>T , CM000678.1:g.1575875G>T	GRCh37
NC_000016.8:g.1515876G>T	NCBI36
NG_032783.1:g.91235C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2768+13C>A MANE Select	ENSP00000406012.2:n.2768+13C>A
ENST00000361339.9:c.350+13C>A	ENSP00000354895.5:n.350+13C>A
ENST00000397417.6:c.*1206+13C>A	ENSP00000380562.2:n.*1206+13C>A
ENST00000426508.6:c.2768+13C>A	ENSP00000406012.2:n.2768+13C>A
ENST00000565298.5:n.1997+13C>A
ENST00000566818.1:n.483+13C>A
NM_014714.3:c.2768+13C>A	NP_055529.2:n.2768+13C>A
XM_006720989.2:c.2768+13C>A	XP_006721052.1:n.2768+13C>A
XM_006720990.2:c.2768+13C>A	XP_006721053.1:n.2768+13C>A
XM_006720991.2:c.2768+13C>A	XP_006721054.1:n.2768+13C>A
XM_006720992.2:c.401+13C>A	XP_006721055.1:n.401+13C>A
XM_011522766.1:c.2522+13C>A	XP_011521068.1:n.2522+13C>A
XM_011522767.1:c.1793+13C>A	XP_011521069.1:n.1793+13C>A
XM_006720990.3:c.2768+13C>A	XP_006721053.1:n.2768+13C>A
XM_006720991.3:c.2768+13C>A	XP_006721054.1:n.2768+13C>A
XM_006720992.3:c.401+13C>A	XP_006721055.1:n.401+13C>A
XM_011522766.3:c.2522+13C>A	XP_011521068.1:n.2522+13C>A
XM_011522767.2:c.1793+13C>A	XP_011521069.1:n.1793+13C>A
XM_017023910.1:c.2768+13C>A	XP_016879399.1:n.2768+13C>A
XM_017023911.1:c.953+13C>A	XP_016879400.1:n.953+13C>A
NM_014714.4:c.2768+13C>A MANE Select	NP_055529.2:n.2768+13C>A