Canonical Allele Identifier: CA1167984966
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1468433679

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059698dup , CM000663.2:g.55059698dup GRCh38
NC_000001.10:g.55525371dup , CM000663.1:g.55525371dup GRCh37
NC_000001.9:g.55297959dup NCBI36
NG_009061.1:g.25152dup , LRG_275:g.25152dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+35dup ENSP00000501161.2:n.1681+35dup
ENST00000710286.1:c.2038+35dup ENSP00000518176.1:n.2038+35dup
ENST00000673903.1:c.1306+35dup ENSP00000501257.1:n.1306+35dup
ENST00000673913.1:c.421+35dup ENSP00000501161.1:n.421+35dup
ENST00000302118.5:c.1681+35dup MANE Select ENSP00000303208.5:n.1681+35dup
ENST00000490692.1:n.2227+1051dup
NM_174936.3:c.1681+35dup , LRG_275t1:c.1681+35dup NP_777596.2:n.1681+35dup
NR_110451.1:n.1288+35dup
XM_011541193.1:c.802+35dup XP_011539495.1:n.802+35dup
NM_174936.4:c.1681+35dup MANE Select NP_777596.2:n.1681+35dup
NR_110451.2:n.1288+35dup