Canonical Allele Identifier: CA493031837

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1573591G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523590G>T , CM000678.2:g.1523590G>T	GRCh38
NC_000016.9:g.1573591G>T , CM000678.1:g.1573591G>T	GRCh37
NC_000016.8:g.1513592G>T	NCBI36
NG_032783.1:g.93519C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3381C>A MANE Select	ENSP00000406012.2:p.Ala1127=
ENST00000361339.9:c.963C>A	ENSP00000354895.5:p.Ala321=
ENST00000397417.6:c.*1819C>A	ENSP00000380562.2:n.*1819C>A
ENST00000426508.6:c.3381C>A	ENSP00000406012.2:p.Ala1127=
ENST00000565298.5:n.3205C>A
NM_014714.3:c.3381C>A	NP_055529.2:p.Ala1127=
XM_006720989.2:c.3381C>A	XP_006721052.1:p.Ala1127=
XM_006720990.2:c.3381C>A	XP_006721053.1:p.Ala1127=
XM_006720991.2:c.3381C>A	XP_006721054.1:p.Ala1127=
XM_006720992.2:c.1014C>A	XP_006721055.1:p.Ala338=
XM_011522766.1:c.3135C>A	XP_011521068.1:p.Ala1045=
XM_011522767.1:c.2406C>A	XP_011521069.1:p.Ala802=
XM_006720990.3:c.3381C>A	XP_006721053.1:p.Ala1127=
XM_006720991.3:c.3381C>A	XP_006721054.1:p.Ala1127=
XM_006720992.3:c.1014C>A	XP_006721055.1:p.Ala338=
XM_011522766.3:c.3135C>A	XP_011521068.1:p.Ala1045=
XM_011522767.2:c.2406C>A	XP_011521069.1:p.Ala802=
XM_017023910.1:c.3381C>A	XP_016879399.1:p.Ala1127=
XM_017023911.1:c.1566C>A	XP_016879400.1:p.Ala522=
NM_014714.4:c.3381C>A MANE Select	NP_055529.2:p.Ala1127=