Canonical Allele Identifier: CA394227084

Gene: IFT140

Linked Data

• gnomAD v4: 16-1525887-T-A
• MyVariant Identifiers: chr16:g.1575888T>A (hg19) ; chr16:g.1525887T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525887T>A , CM000678.2:g.1525887T>A	GRCh38
NC_000016.9:g.1575888T>A , CM000678.1:g.1575888T>A	GRCh37
NC_000016.8:g.1515889T>A	NCBI36
NG_032783.1:g.91222A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2768A>T MANE Select	ENSP00000406012.2:p.Tyr923Phe
ENST00000361339.9:c.350A>T	ENSP00000354895.5:p.Tyr117Phe
ENST00000397417.6:c.*1206A>T	ENSP00000380562.2:n.*1206A>T
ENST00000426508.6:c.2768A>T	ENSP00000406012.2:p.Tyr923Phe
ENST00000565298.5:n.1997A>T
ENST00000566818.1:n.483A>T
NM_014714.3:c.2768A>T	NP_055529.2:p.Tyr923Phe
XM_006720989.2:c.2768A>T	XP_006721052.1:p.Tyr923Phe
XM_006720990.2:c.2768A>T	XP_006721053.1:p.Tyr923Phe
XM_006720991.2:c.2768A>T	XP_006721054.1:p.Tyr923Phe
XM_006720992.2:c.401A>T	XP_006721055.1:p.Tyr134Phe
XM_011522766.1:c.2522A>T	XP_011521068.1:p.Tyr841Phe
XM_011522767.1:c.1793A>T	XP_011521069.1:p.Tyr598Phe
XM_006720990.3:c.2768A>T	XP_006721053.1:p.Tyr923Phe
XM_006720991.3:c.2768A>T	XP_006721054.1:p.Tyr923Phe
XM_006720992.3:c.401A>T	XP_006721055.1:p.Tyr134Phe
XM_011522766.3:c.2522A>T	XP_011521068.1:p.Tyr841Phe
XM_011522767.2:c.1793A>T	XP_011521069.1:p.Tyr598Phe
XM_017023910.1:c.2768A>T	XP_016879399.1:p.Tyr923Phe
XM_017023911.1:c.953A>T	XP_016879400.1:p.Tyr318Phe
NM_014714.4:c.2768A>T MANE Select	NP_055529.2:p.Tyr923Phe