Canonical Allele Identifier: CA340480759

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529151G>C (hg19) ; chr1:g.55063478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063478G>C , CM000663.2:g.55063478G>C	GRCh38
NC_000001.10:g.55529151G>C , CM000663.1:g.55529151G>C	GRCh37
NC_000001.9:g.55301739G>C	NCBI36
NG_009061.1:g.28932G>C , LRG_275:g.28932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*313G>C	ENSP00000501161.2:n.*313G>C
ENST00000710286.1:c.2330G>C	ENSP00000518176.1:p.Ser777Thr
ENST00000673903.1:c.1598G>C	ENSP00000501257.1:p.Ser533Thr
ENST00000673913.1:c.823G>C	ENSP00000501161.1:n.823G>C
ENST00000302118.5:c.1973G>C MANE Select	ENSP00000303208.5:p.Ser658Thr
ENST00000490692.1:n.2519G>C
NM_174936.3:c.1973G>C , LRG_275t1:c.1973G>C	NP_777596.2:p.Ser658Thr
NR_110451.1:n.1580G>C
XM_011541193.1:c.1094G>C	XP_011539495.1:p.Ser365Thr
NM_174936.4:c.1973G>C MANE Select	NP_777596.2:p.Ser658Thr
NR_110451.2:n.1580G>C