Canonical Allele Identifier: CA394225508

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1573693G>T (hg19) ; chr16:g.1523692G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1523692G>T , CM000678.2:g.1523692G>T	GRCh38
NC_000016.9:g.1573693G>T , CM000678.1:g.1573693G>T	GRCh37
NC_000016.8:g.1513694G>T	NCBI36
NG_032783.1:g.93417C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3279C>A MANE Select	ENSP00000406012.2:p.His1093Gln
ENST00000361339.9:c.861C>A	ENSP00000354895.5:p.His287Gln
ENST00000397417.6:c.*1717C>A	ENSP00000380562.2:n.*1717C>A
ENST00000426508.6:c.3279C>A	ENSP00000406012.2:p.His1093Gln
ENST00000565298.5:n.3103C>A
NM_014714.3:c.3279C>A	NP_055529.2:p.His1093Gln
XM_006720989.2:c.3279C>A	XP_006721052.1:p.His1093Gln
XM_006720990.2:c.3279C>A	XP_006721053.1:p.His1093Gln
XM_006720991.2:c.3279C>A	XP_006721054.1:p.His1093Gln
XM_006720992.2:c.912C>A	XP_006721055.1:p.His304Gln
XM_011522766.1:c.3033C>A	XP_011521068.1:p.His1011Gln
XM_011522767.1:c.2304C>A	XP_011521069.1:p.His768Gln
XM_006720990.3:c.3279C>A	XP_006721053.1:p.His1093Gln
XM_006720991.3:c.3279C>A	XP_006721054.1:p.His1093Gln
XM_006720992.3:c.912C>A	XP_006721055.1:p.His304Gln
XM_011522766.3:c.3033C>A	XP_011521068.1:p.His1011Gln
XM_011522767.2:c.2304C>A	XP_011521069.1:p.His768Gln
XM_017023910.1:c.3279C>A	XP_016879399.1:p.His1093Gln
XM_017023911.1:c.1464C>A	XP_016879400.1:p.His488Gln
NM_014714.4:c.3279C>A MANE Select	NP_055529.2:p.His1093Gln