Canonical Allele Identifier: CA7813505

Gene: IFT140

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525897C>A , CM000678.2:g.1525897C>A	GRCh38
NC_000016.9:g.1575898C>A , CM000678.1:g.1575898C>A	GRCh37
NC_000016.8:g.1515899C>A	NCBI36
NG_032783.1:g.91212G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014714.4:c.2758G>T MANE Select	NP_055529.2:p.Ala920Ser
ENST00000426508.7:c.2758G>T MANE Select	ENSP00000406012.2:p.Ala920Ser
NM_014714.3:c.2758G>T	NP_055529.2:p.Ala920Ser
ENST00000361339.9:c.340G>T	ENSP00000354895.5:p.Ala114Ser
ENST00000397417.6:c.*1196G>T	ENSP00000380562.2:n.*1196G>T
ENST00000426508.6:c.2758G>T	ENSP00000406012.2:p.Ala920Ser
ENST00000565298.5:n.1987G>T
ENST00000566818.1:n.473G>T
XM_006720989.2:c.2758G>T	XP_006721052.1:p.Ala920Ser
XM_006720990.2:c.2758G>T	XP_006721053.1:p.Ala920Ser
XM_006720990.3:c.2758G>T	XP_006721053.1:p.Ala920Ser
XM_006720991.2:c.2758G>T	XP_006721054.1:p.Ala920Ser
XM_006720991.3:c.2758G>T	XP_006721054.1:p.Ala920Ser
XM_006720992.2:c.391G>T	XP_006721055.1:p.Ala131Ser
XM_006720992.3:c.391G>T	XP_006721055.1:p.Ala131Ser
XM_011522766.1:c.2512G>T	XP_011521068.1:p.Ala838Ser
XM_011522766.3:c.2512G>T	XP_011521068.1:p.Ala838Ser
XM_011522767.1:c.1783G>T	XP_011521069.1:p.Ala595Ser
XM_011522767.2:c.1783G>T	XP_011521069.1:p.Ala595Ser
XM_017023910.1:c.2758G>T	XP_016879399.1:p.Ala920Ser
XM_017023911.1:c.943G>T	XP_016879400.1:p.Ala315Ser