Canonical Allele Identifier: CA394225118

Gene: IFT140

Linked Data

• gnomAD v4: 16-1520805-G-C
• MyVariant Identifiers: chr16:g.1570806G>C (hg19) ; chr16:g.1520805G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520805G>C , CM000678.2:g.1520805G>C	GRCh38
NC_000016.9:g.1570806G>C , CM000678.1:g.1570806G>C	GRCh37
NC_000016.8:g.1510807G>C	NCBI36
NG_032783.1:g.96304C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3457C>G MANE Select	ENSP00000406012.2:p.Gln1153Glu
ENST00000361339.9:c.1039C>G	ENSP00000354895.5:p.Gln347Glu
ENST00000397417.6:c.*1895C>G	ENSP00000380562.2:n.*1895C>G
ENST00000426508.6:c.3457C>G	ENSP00000406012.2:p.Gln1153Glu
ENST00000565298.5:n.3281C>G
NM_014714.3:c.3457C>G	NP_055529.2:p.Gln1153Glu
XM_006720989.2:c.3457C>G	XP_006721052.1:p.Gln1153Glu
XM_006720990.2:c.3457C>G	XP_006721053.1:p.Gln1153Glu
XM_006720991.2:c.3457C>G	XP_006721054.1:p.Gln1153Glu
XM_006720992.2:c.1090C>G	XP_006721055.1:p.Gln364Glu
XM_011522766.1:c.3211C>G	XP_011521068.1:p.Gln1071Glu
XM_011522767.1:c.2482C>G	XP_011521069.1:p.Gln828Glu
XM_006720990.3:c.3457C>G	XP_006721053.1:p.Gln1153Glu
XM_006720991.3:c.3457C>G	XP_006721054.1:p.Gln1153Glu
XM_006720992.3:c.1090C>G	XP_006721055.1:p.Gln364Glu
XM_011522766.3:c.3211C>G	XP_011521068.1:p.Gln1071Glu
XM_011522767.2:c.2482C>G	XP_011521069.1:p.Gln828Glu
XM_017023910.1:c.3457C>G	XP_016879399.1:p.Gln1153Glu
XM_017023911.1:c.1642C>G	XP_016879400.1:p.Gln548Glu
NM_014714.4:c.3457C>G MANE Select	NP_055529.2:p.Gln1153Glu