Canonical Allele Identifier: CA394227404

Gene: IFT140

Linked Data

• MyVariant Identifiers: chr16:g.1575974G>C (hg19) ; chr16:g.1525973G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1525973G>C , CM000678.2:g.1525973G>C	GRCh38
NC_000016.9:g.1575974G>C , CM000678.1:g.1575974G>C	GRCh37
NC_000016.8:g.1515975G>C	NCBI36
NG_032783.1:g.91136C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426508.7:c.2682C>G MANE Select	ENSP00000406012.2:p.His894Gln
ENST00000361339.9:c.264C>G	ENSP00000354895.5:p.His88Gln
ENST00000397417.6:c.*1120C>G	ENSP00000380562.2:n.*1120C>G
ENST00000426508.6:c.2682C>G	ENSP00000406012.2:p.His894Gln
ENST00000565298.5:n.1911C>G
ENST00000566818.1:n.397C>G
NM_014714.3:c.2682C>G	NP_055529.2:p.His894Gln
XM_006720989.2:c.2682C>G	XP_006721052.1:p.His894Gln
XM_006720990.2:c.2682C>G	XP_006721053.1:p.His894Gln
XM_006720991.2:c.2682C>G	XP_006721054.1:p.His894Gln
XM_006720992.2:c.315C>G	XP_006721055.1:p.His105Gln
XM_011522766.1:c.2436C>G	XP_011521068.1:p.His812Gln
XM_011522767.1:c.1707C>G	XP_011521069.1:p.His569Gln
XM_006720990.3:c.2682C>G	XP_006721053.1:p.His894Gln
XM_006720991.3:c.2682C>G	XP_006721054.1:p.His894Gln
XM_006720992.3:c.315C>G	XP_006721055.1:p.His105Gln
XM_011522766.3:c.2436C>G	XP_011521068.1:p.His812Gln
XM_011522767.2:c.1707C>G	XP_011521069.1:p.His569Gln
XM_017023910.1:c.2682C>G	XP_016879399.1:p.His894Gln
XM_017023911.1:c.867C>G	XP_016879400.1:p.His289Gln
NM_014714.4:c.2682C>G MANE Select	NP_055529.2:p.His894Gln