Canonical Allele Identifier: CA492931921

Gene: IFT140

Linked Data

• dbSNP Id: rs2141147957
• MyVariant Identifiers: chr16:g.1570747T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1520746T>C , CM000678.2:g.1520746T>C	GRCh38
NC_000016.9:g.1570747T>C , CM000678.1:g.1570747T>C	GRCh37
NC_000016.8:g.1510748T>C	NCBI36
NG_032783.1:g.96363A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426508.7:c.3516A>G MANE Select	ENSP00000406012.2:p.Glu1172=
ENST00000361339.9:c.1098A>G	ENSP00000354895.5:p.Glu366=
ENST00000397417.6:c.*1954A>G	ENSP00000380562.2:n.*1954A>G
ENST00000426508.6:c.3516A>G	ENSP00000406012.2:p.Glu1172=
ENST00000565298.5:n.3340A>G
NM_014714.3:c.3516A>G	NP_055529.2:p.Glu1172=
XM_006720989.2:c.3516A>G	XP_006721052.1:p.Glu1172=
XM_006720990.2:c.3516A>G	XP_006721053.1:p.Glu1172=
XM_006720991.2:c.3516A>G	XP_006721054.1:p.Glu1172=
XM_006720992.2:c.1149A>G	XP_006721055.1:p.Glu383=
XM_011522766.1:c.3270A>G	XP_011521068.1:p.Glu1090=
XM_011522767.1:c.2541A>G	XP_011521069.1:p.Glu847=
XM_006720990.3:c.3516A>G	XP_006721053.1:p.Glu1172=
XM_006720991.3:c.3516A>G	XP_006721054.1:p.Glu1172=
XM_006720992.3:c.1149A>G	XP_006721055.1:p.Glu383=
XM_011522766.3:c.3270A>G	XP_011521068.1:p.Glu1090=
XM_011522767.2:c.2541A>G	XP_011521069.1:p.Glu847=
XM_017023910.1:c.3516A>G	XP_016879399.1:p.Glu1172=
XM_017023911.1:c.1701A>G	XP_016879400.1:p.Glu567=
NM_014714.4:c.3516A>G MANE Select	NP_055529.2:p.Glu1172=