Canonical Allele Identifier: CA340480011
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059610A>C , CM000663.2:g.55059610A>C GRCh38
NC_000001.10:g.55525283A>C , CM000663.1:g.55525283A>C GRCh37
NC_000001.9:g.55297871A>C NCBI36
NG_009061.1:g.25064A>C , LRG_275:g.25064A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1628A>C ENSP00000501161.2:p.Glu543Ala
ENST00000710286.1:c.1985A>C ENSP00000518176.1:p.Glu662Ala
ENST00000673903.1:c.1253A>C ENSP00000501257.1:p.Glu418Ala
ENST00000673913.1:c.368A>C ENSP00000501161.1:p.Glu123Ala
ENST00000302118.5:c.1628A>C MANE Select ENSP00000303208.5:p.Glu543Ala
ENST00000490692.1:n.2227+963A>C
NM_174936.3:c.1628A>C , LRG_275t1:c.1628A>C NP_777596.2:p.Glu543Ala
NR_110451.1:n.1235A>C
XM_011541193.1:c.749A>C XP_011539495.1:p.Glu250Ala
NM_174936.4:c.1628A>C MANE Select NP_777596.2:p.Glu543Ala
NR_110451.2:n.1235A>C