Canonical Allele Identifier: CA493031434

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1570168C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520167C>A , CM000678.2:g.1520167C>A	GRCh38
NC_000016.9:g.1570168C>A , CM000678.1:g.1570168C>A	GRCh37
NC_000016.8:g.1510169C>A	NCBI36
NG_032783.1:g.96942G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.3837G>T MANE Select	ENSP00000406012.2:p.Leu1279=
ENST00000361339.9:c.1419G>T	ENSP00000354895.5:p.Leu473=
ENST00000397417.6:c.*2275G>T	ENSP00000380562.2:n.*2275G>T
ENST00000426508.6:c.3837G>T	ENSP00000406012.2:p.Leu1279=
ENST00000565298.5:n.3661G>T
NM_014714.3:c.3837G>T	NP_055529.2:p.Leu1279=
XM_006720989.2:c.3837G>T	XP_006721052.1:p.Leu1279=
XM_006720990.2:c.3837G>T	XP_006721053.1:p.Leu1279=
XM_006720991.2:c.3837G>T	XP_006721054.1:p.Leu1279=
XM_006720992.2:c.1470G>T	XP_006721055.1:p.Leu490=
XM_011522766.1:c.3591G>T	XP_011521068.1:p.Leu1197=
XM_011522767.1:c.2862G>T	XP_011521069.1:p.Leu954=
XM_006720990.3:c.3837G>T	XP_006721053.1:p.Leu1279=
XM_006720991.3:c.3837G>T	XP_006721054.1:p.Leu1279=
XM_006720992.3:c.1470G>T	XP_006721055.1:p.Leu490=
XM_011522766.3:c.3591G>T	XP_011521068.1:p.Leu1197=
XM_011522767.2:c.2862G>T	XP_011521069.1:p.Leu954=
XM_017023910.1:c.3837G>T	XP_016879399.1:p.Leu1279=
XM_017023911.1:c.2022G>T	XP_016879400.1:p.Leu674=
NM_014714.4:c.3837G>T MANE Select	NP_055529.2:p.Leu1279=