Canonical Allele Identifier: CA1167986619
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644780631
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063694dup , CM000663.2:g.55063694dup GRCh38
NC_000001.10:g.55529367dup , CM000663.1:g.55529367dup GRCh37
NC_000001.9:g.55301955dup NCBI36
NG_009061.1:g.29148dup , LRG_275:g.29148dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*529dup ENSP00000501161.2:n.*529dup
ENST00000710286.1:c.*110dup ENSP00000518176.1:n.*110dup
ENST00000673903.1:c.*110dup ENSP00000501257.1:n.*110dup
ENST00000302118.5:c.*110dup MANE Select ENSP00000303208.5:n.*110dup
ENST00000490692.1:n.2735dup
NM_174936.3:c.*110dup , LRG_275t1:c.*110dup NP_777596.2:n.*110dup
NR_110451.1:n.1796dup
XM_011541193.1:c.*110dup XP_011539495.1:n.*110dup
NM_174936.4:c.*110dup MANE Select NP_777596.2:n.*110dup
NR_110451.2:n.1796dup
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