Canonical Allele Identifier: CA394225383

Gene: IFT140

Linked Data

• gnomAD v4: 16-1523634-T-C
• MyVariant Identifiers: chr16:g.1573635T>C (hg19) ; chr16:g.1523634T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523634T>C , CM000678.2:g.1523634T>C	GRCh38
NC_000016.9:g.1573635T>C , CM000678.1:g.1573635T>C	GRCh37
NC_000016.8:g.1513636T>C	NCBI36
NG_032783.1:g.93475A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3337A>G MANE Select	ENSP00000406012.2:p.Ile1113Val
ENST00000361339.9:c.919A>G	ENSP00000354895.5:p.Ile307Val
ENST00000397417.6:c.*1775A>G	ENSP00000380562.2:n.*1775A>G
ENST00000426508.6:c.3337A>G	ENSP00000406012.2:p.Ile1113Val
ENST00000565298.5:n.3161A>G
NM_014714.3:c.3337A>G	NP_055529.2:p.Ile1113Val
XM_006720989.2:c.3337A>G	XP_006721052.1:p.Ile1113Val
XM_006720990.2:c.3337A>G	XP_006721053.1:p.Ile1113Val
XM_006720991.2:c.3337A>G	XP_006721054.1:p.Ile1113Val
XM_006720992.2:c.970A>G	XP_006721055.1:p.Ile324Val
XM_011522766.1:c.3091A>G	XP_011521068.1:p.Ile1031Val
XM_011522767.1:c.2362A>G	XP_011521069.1:p.Ile788Val
XM_006720990.3:c.3337A>G	XP_006721053.1:p.Ile1113Val
XM_006720991.3:c.3337A>G	XP_006721054.1:p.Ile1113Val
XM_006720992.3:c.970A>G	XP_006721055.1:p.Ile324Val
XM_011522766.3:c.3091A>G	XP_011521068.1:p.Ile1031Val
XM_011522767.2:c.2362A>G	XP_011521069.1:p.Ile788Val
XM_017023910.1:c.3337A>G	XP_016879399.1:p.Ile1113Val
XM_017023911.1:c.1522A>G	XP_016879400.1:p.Ile508Val
NM_014714.4:c.3337A>G MANE Select	NP_055529.2:p.Ile1113Val