Canonical Allele Identifier: CA394205983

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1616211G>C (hg19) ; chr16:g.1566210G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1566210G>C , CM000678.2:g.1566210G>C	GRCh38
NC_000016.9:g.1616211G>C , CM000678.1:g.1616211G>C	GRCh37
NC_000016.8:g.1556212G>C	NCBI36
NG_032783.1:g.50899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.1852C>G MANE Select	ENSP00000406012.2:p.Gln618Glu
ENST00000397417.6:c.*404C>G	ENSP00000380562.2:n.*404C>G
ENST00000426508.6:c.1852C>G	ENSP00000406012.2:p.Gln618Glu
ENST00000439987.6:n.1913C>G
ENST00000565298.5:n.540C>G
NM_014714.3:c.1852C>G	NP_055529.2:p.Gln618Glu
XM_005255725.3:c.1852C>G	XP_005255782.1:p.Gln618Glu
XM_005255726.2:c.1852C>G	XP_005255783.1:p.Gln618Glu
XM_006720989.2:c.1852C>G	XP_006721052.1:p.Gln618Glu
XM_006720990.2:c.1852C>G	XP_006721053.1:p.Gln618Glu
XM_006720991.2:c.1852C>G	XP_006721054.1:p.Gln618Glu
XM_011522766.1:c.1606C>G	XP_011521068.1:p.Gln536Glu
XM_011522767.1:c.877C>G	XP_011521069.1:p.Gln293Glu
XM_011522768.1:c.1852C>G	XP_011521070.1:p.Gln618Glu
XM_011522769.1:c.1852C>G	XP_011521071.1:p.Gln618Glu
XM_011522771.1:c.1852C>G	XP_011521073.1:p.Gln618Glu
XM_011522772.1:c.1852C>G	XP_011521074.1:p.Gln618Glu
XM_005255725.5:c.1852C>G	XP_005255782.1:p.Gln618Glu
XM_005255726.4:c.1852C>G	XP_005255783.1:p.Gln618Glu
XM_006720990.3:c.1852C>G	XP_006721053.1:p.Gln618Glu
XM_006720991.3:c.1852C>G	XP_006721054.1:p.Gln618Glu
XM_011522766.3:c.1606C>G	XP_011521068.1:p.Gln536Glu
XM_011522767.2:c.877C>G	XP_011521069.1:p.Gln293Glu
XM_011522769.3:c.1852C>G	XP_011521071.1:p.Gln618Glu
XM_011522771.3:c.1852C>G	XP_011521073.1:p.Gln618Glu
XM_011522772.3:c.1852C>G	XP_011521074.1:p.Gln618Glu
XM_017023910.1:c.1852C>G	XP_016879399.1:p.Gln618Glu
XM_017023911.1:c.37C>G	XP_016879400.1:p.Gln13Glu
NM_014714.4:c.1852C>G MANE Select	NP_055529.2:p.Gln618Glu