Canonical Allele Identifier: CA493031982

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1573648C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523647C>T , CM000678.2:g.1523647C>T	GRCh38
NC_000016.9:g.1573648C>T , CM000678.1:g.1573648C>T	GRCh37
NC_000016.8:g.1513649C>T	NCBI36
NG_032783.1:g.93462G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3324G>A MANE Select	ENSP00000406012.2:p.Val1108=
ENST00000361339.9:c.906G>A	ENSP00000354895.5:p.Val302=
ENST00000397417.6:c.*1762G>A	ENSP00000380562.2:n.*1762G>A
ENST00000426508.6:c.3324G>A	ENSP00000406012.2:p.Val1108=
ENST00000565298.5:n.3148G>A
NM_014714.3:c.3324G>A	NP_055529.2:p.Val1108=
XM_006720989.2:c.3324G>A	XP_006721052.1:p.Val1108=
XM_006720990.2:c.3324G>A	XP_006721053.1:p.Val1108=
XM_006720991.2:c.3324G>A	XP_006721054.1:p.Val1108=
XM_006720992.2:c.957G>A	XP_006721055.1:p.Val319=
XM_011522766.1:c.3078G>A	XP_011521068.1:p.Val1026=
XM_011522767.1:c.2349G>A	XP_011521069.1:p.Val783=
XM_006720990.3:c.3324G>A	XP_006721053.1:p.Val1108=
XM_006720991.3:c.3324G>A	XP_006721054.1:p.Val1108=
XM_006720992.3:c.957G>A	XP_006721055.1:p.Val319=
XM_011522766.3:c.3078G>A	XP_011521068.1:p.Val1026=
XM_011522767.2:c.2349G>A	XP_011521069.1:p.Val783=
XM_017023910.1:c.3324G>A	XP_016879399.1:p.Val1108=
XM_017023911.1:c.1509G>A	XP_016879400.1:p.Val503=
NM_014714.4:c.3324G>A MANE Select	NP_055529.2:p.Val1108=