Canonical Allele Identifier: CA394227438

Gene: IFT140

Linked Data

• dbSNP Id: rs1596305892
• MyVariant Identifiers: chr16:g.1575984A>C (hg19) ; chr16:g.1525983A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525983A>C , CM000678.2:g.1525983A>C	GRCh38
NC_000016.9:g.1575984A>C , CM000678.1:g.1575984A>C	GRCh37
NC_000016.8:g.1515985A>C	NCBI36
NG_032783.1:g.91126T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2672T>G MANE Select	ENSP00000406012.2:p.Val891Gly
ENST00000361339.9:c.254T>G	ENSP00000354895.5:p.Val85Gly
ENST00000397417.6:c.*1110T>G	ENSP00000380562.2:n.*1110T>G
ENST00000426508.6:c.2672T>G	ENSP00000406012.2:p.Val891Gly
ENST00000565298.5:n.1901T>G
ENST00000566818.1:n.387T>G
NM_014714.3:c.2672T>G	NP_055529.2:p.Val891Gly
XM_006720989.2:c.2672T>G	XP_006721052.1:p.Val891Gly
XM_006720990.2:c.2672T>G	XP_006721053.1:p.Val891Gly
XM_006720991.2:c.2672T>G	XP_006721054.1:p.Val891Gly
XM_006720992.2:c.305T>G	XP_006721055.1:p.Val102Gly
XM_011522766.1:c.2426T>G	XP_011521068.1:p.Val809Gly
XM_011522767.1:c.1697T>G	XP_011521069.1:p.Val566Gly
XM_006720990.3:c.2672T>G	XP_006721053.1:p.Val891Gly
XM_006720991.3:c.2672T>G	XP_006721054.1:p.Val891Gly
XM_006720992.3:c.305T>G	XP_006721055.1:p.Val102Gly
XM_011522766.3:c.2426T>G	XP_011521068.1:p.Val809Gly
XM_011522767.2:c.1697T>G	XP_011521069.1:p.Val566Gly
XM_017023910.1:c.2672T>G	XP_016879399.1:p.Val891Gly
XM_017023911.1:c.857T>G	XP_016879400.1:p.Val286Gly
NM_014714.4:c.2672T>G MANE Select	NP_055529.2:p.Val891Gly