Canonical Allele Identifier: CA340480634

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529085G>C (hg19) ; chr1:g.55063412G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063412G>C , CM000663.2:g.55063412G>C	GRCh38
NC_000001.10:g.55529085G>C , CM000663.1:g.55529085G>C	GRCh37
NC_000001.9:g.55301673G>C	NCBI36
NG_009061.1:g.28866G>C , LRG_275:g.28866G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000673913.2:c.*247G>C	ENSP00000501161.2:n.*247G>C
ENST00000710286.1:c.2264G>C	ENSP00000518176.1:p.Ser755Thr
ENST00000673903.1:c.1532G>C	ENSP00000501257.1:p.Ser511Thr
ENST00000673913.1:c.757G>C	ENSP00000501161.1:n.757G>C
ENST00000302118.5:c.1907G>C MANE Select	ENSP00000303208.5:p.Ser636Thr
ENST00000490692.1:n.2453G>C
NM_174936.3:c.1907G>C , LRG_275t1:c.1907G>C	NP_777596.2:p.Ser636Thr
NR_110451.1:n.1514G>C
XM_011541193.1:c.1028G>C	XP_011539495.1:p.Ser343Thr
NM_174936.4:c.1907G>C MANE Select	NP_777596.2:p.Ser636Thr
NR_110451.2:n.1514G>C