Canonical Allele Identifier: CA340480491
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061534G>C , CM000663.2:g.55061534G>C GRCh38
NC_000001.10:g.55527207G>C , CM000663.1:g.55527207G>C GRCh37
NC_000001.9:g.55299795G>C NCBI36
NG_009061.1:g.26988G>C , LRG_275:g.26988G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*181G>C ENSP00000501161.2:n.*181G>C
ENST00000710286.1:c.2198G>C ENSP00000518176.1:p.Gly733Ala
ENST00000673903.1:c.1466G>C ENSP00000501257.1:p.Gly489Ala
ENST00000673913.1:c.691G>C ENSP00000501161.1:n.691G>C
ENST00000302118.5:c.1841G>C MANE Select ENSP00000303208.5:p.Gly614Ala
ENST00000490692.1:n.2387G>C
NM_174936.3:c.1841G>C , LRG_275t1:c.1841G>C NP_777596.2:p.Gly614Ala
NR_110451.1:n.1448G>C
XM_011541193.1:c.962G>C XP_011539495.1:p.Gly321Ala
NM_174936.4:c.1841G>C MANE Select NP_777596.2:p.Gly614Ala
NR_110451.2:n.1448G>C