Canonical Allele Identifier: CA7813617

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1526721C>A , CM000678.2:g.1526721C>A	GRCh38
NC_000016.9:g.1576722C>A , CM000678.1:g.1576722C>A	GRCh37
NC_000016.8:g.1516723C>A	NCBI36
NG_032783.1:g.90388G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.2475G>T MANE Select	NP_055529.2:p.Gly825=
ENST00000426508.7:c.2475G>T MANE Select	ENSP00000406012.2:p.Gly825=
NM_014714.3:c.2475G>T	NP_055529.2:p.Gly825=
ENST00000361339.9:c.57G>T	ENSP00000354895.5:p.Gly19=
ENST00000397417.6:c.*1015+12G>T	ENSP00000380562.2:n.*1015+12G>T
ENST00000426508.6:c.2475G>T	ENSP00000406012.2:p.Gly825=
ENST00000565298.5:n.1163G>T
ENST00000566818.1:n.292+12G>T
XM_006720989.2:c.2475G>T	XP_006721052.1:p.Gly825=
XM_006720990.2:c.2475G>T	XP_006721053.1:p.Gly825=
XM_006720990.3:c.2475G>T	XP_006721053.1:p.Gly825=
XM_006720991.2:c.2475G>T	XP_006721054.1:p.Gly825=
XM_006720991.3:c.2475G>T	XP_006721054.1:p.Gly825=
XM_006720992.2:c.108G>T	XP_006721055.1:p.Gly36=
XM_006720992.3:c.108G>T	XP_006721055.1:p.Gly36=
XM_011522766.1:c.2229G>T	XP_011521068.1:p.Gly743=
XM_011522766.3:c.2229G>T	XP_011521068.1:p.Gly743=
XM_011522767.1:c.1500G>T	XP_011521069.1:p.Gly500=
XM_011522767.2:c.1500G>T	XP_011521069.1:p.Gly500=
XM_017023910.1:c.2475G>T	XP_016879399.1:p.Gly825=
XM_017023911.1:c.660G>T	XP_016879400.1:p.Gly220=