Canonical Allele Identifier: CA394227437

Gene: IFT140

Linked Data

• gnomAD v4: 16-1525981-C-A
• MyVariant Identifiers: chr16:g.1575982C>A (hg19) ; chr16:g.1525981C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525981C>A , CM000678.2:g.1525981C>A	GRCh38
NC_000016.9:g.1575982C>A , CM000678.1:g.1575982C>A	GRCh37
NC_000016.8:g.1515983C>A	NCBI36
NG_032783.1:g.91128G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2674G>T MANE Select	ENSP00000406012.2:p.Ala892Ser
ENST00000361339.9:c.256G>T	ENSP00000354895.5:p.Ala86Ser
ENST00000397417.6:c.*1112G>T	ENSP00000380562.2:n.*1112G>T
ENST00000426508.6:c.2674G>T	ENSP00000406012.2:p.Ala892Ser
ENST00000565298.5:n.1903G>T
ENST00000566818.1:n.389G>T
NM_014714.3:c.2674G>T	NP_055529.2:p.Ala892Ser
XM_006720989.2:c.2674G>T	XP_006721052.1:p.Ala892Ser
XM_006720990.2:c.2674G>T	XP_006721053.1:p.Ala892Ser
XM_006720991.2:c.2674G>T	XP_006721054.1:p.Ala892Ser
XM_006720992.2:c.307G>T	XP_006721055.1:p.Ala103Ser
XM_011522766.1:c.2428G>T	XP_011521068.1:p.Ala810Ser
XM_011522767.1:c.1699G>T	XP_011521069.1:p.Ala567Ser
XM_006720990.3:c.2674G>T	XP_006721053.1:p.Ala892Ser
XM_006720991.3:c.2674G>T	XP_006721054.1:p.Ala892Ser
XM_006720992.3:c.307G>T	XP_006721055.1:p.Ala103Ser
XM_011522766.3:c.2428G>T	XP_011521068.1:p.Ala810Ser
XM_011522767.2:c.1699G>T	XP_011521069.1:p.Ala567Ser
XM_017023910.1:c.2674G>T	XP_016879399.1:p.Ala892Ser
XM_017023911.1:c.859G>T	XP_016879400.1:p.Ala287Ser
NM_014714.4:c.2674G>T MANE Select	NP_055529.2:p.Ala892Ser