Canonical Allele Identifier: CA1167978052

Gene: PCSK9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55043747_55043749delinsCTT , CM000663.2:g.55043747_55043749delinsCTT	GRCh38
NC_000001.10:g.55509420_55509422delinsCTT , CM000663.1:g.55509420_55509422delinsCTT	GRCh37
NC_000001.9:g.55282008_55282010delinsCTT	NCBI36
NG_009061.1:g.9201_9203delinsCTT , LRG_275:g.9201_9203delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.208-96_208-94delinsCTT	ENSP00000501161.2:n.208-96_208-94delinsCTT
ENST00000710286.1:c.565-96_565-94delinsCTT	ENSP00000518176.1:n.565-96_565-94delinsCTT
ENST00000673726.1:c.208-96_208-94delinsCTT	ENSP00000501004.1:n.208-96_208-94delinsCTT
ENST00000673903.1:c.-168-96_-168-94delinsCTT	ENSP00000501257.1:n.-168-96_-168-94delinsCTT
ENST00000302118.5:c.208-96_208-94delinsCTT MANE Select	ENSP00000303208.5:n.208-96_208-94delinsCTT
NM_174936.3:c.208-96_208-94delinsCTT , LRG_275t1:c.208-96_208-94delinsCTT	NP_777596.2:n.208-96_208-94delinsCTT
NR_110451.1:n.182+3344_182+3346delinsCTT
NM_174936.4:c.208-96_208-94delinsCTT MANE Select	NP_777596.2:n.208-96_208-94delinsCTT
NR_110451.2:n.182+3344_182+3346delinsCTT