Canonical Allele Identifier: CA340480776

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529163G>C (hg19) ; chr1:g.55063490G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063490G>C , CM000663.2:g.55063490G>C	GRCh38
NC_000001.10:g.55529163G>C , CM000663.1:g.55529163G>C	GRCh37
NC_000001.9:g.55301751G>C	NCBI36
NG_009061.1:g.28944G>C , LRG_275:g.28944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*325G>C	ENSP00000501161.2:n.*325G>C
ENST00000710286.1:c.2342G>C	ENSP00000518176.1:p.Ser781Thr
ENST00000673903.1:c.1610G>C	ENSP00000501257.1:p.Ser537Thr
ENST00000673913.1:c.835G>C	ENSP00000501161.1:n.835G>C
ENST00000302118.5:c.1985G>C MANE Select	ENSP00000303208.5:p.Ser662Thr
ENST00000490692.1:n.2531G>C
NM_174936.3:c.1985G>C , LRG_275t1:c.1985G>C	NP_777596.2:p.Ser662Thr
NR_110451.1:n.1592G>C
XM_011541193.1:c.1106G>C	XP_011539495.1:p.Ser369Thr
NM_174936.4:c.1985G>C MANE Select	NP_777596.2:p.Ser662Thr
NR_110451.2:n.1592G>C