Canonical Allele Identifier: CA340479963
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059586G>C , CM000663.2:g.55059586G>C GRCh38
NC_000001.10:g.55525259G>C , CM000663.1:g.55525259G>C GRCh37
NC_000001.9:g.55297847G>C NCBI36
NG_009061.1:g.25040G>C , LRG_275:g.25040G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1604G>C ENSP00000501161.2:p.Ser535Thr
ENST00000710286.1:c.1961G>C ENSP00000518176.1:p.Ser654Thr
ENST00000673903.1:c.1229G>C ENSP00000501257.1:p.Ser410Thr
ENST00000673913.1:c.344G>C ENSP00000501161.1:p.Ser115Thr
ENST00000302118.5:c.1604G>C MANE Select ENSP00000303208.5:p.Ser535Thr
ENST00000490692.1:n.2227+939G>C
NM_174936.3:c.1604G>C , LRG_275t1:c.1604G>C NP_777596.2:p.Ser535Thr
NR_110451.1:n.1211G>C
XM_011541193.1:c.725G>C XP_011539495.1:p.Ser242Thr
NM_174936.4:c.1604G>C MANE Select NP_777596.2:p.Ser535Thr
NR_110451.2:n.1211G>C