Canonical Allele Identifier: CA1149036903
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061728G= , CM000663.2:g.55061728G= GRCh38
NC_000001.10:g.55527401G= , CM000663.1:g.55527401G= GRCh37
NC_000001.9:g.55299989G= NCBI36
NG_009061.1:g.27182G= , LRG_275:g.27182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+172G= ENSP00000501161.2:n.*203+172G=
ENST00000710286.1:c.2220+172G= ENSP00000518176.1:n.2220+172G=
ENST00000673903.1:c.1488+172G= ENSP00000501257.1:n.1488+172G=
ENST00000673913.1:c.713+172G= ENSP00000501161.1:n.713+172G=
ENST00000302118.5:c.1863+172G= MANE Select ENSP00000303208.5:n.1863+172G=
ENST00000490692.1:n.2409+172G=
NM_174936.3:c.1863+172G= , LRG_275t1:c.1863+172G= NP_777596.2:n.1863+172G=
NR_110451.1:n.1470+172G=
XM_011541193.1:c.984+172G= XP_011539495.1:n.984+172G=
NM_174936.4:c.1863+172G= MANE Select NP_777596.2:n.1863+172G=
NR_110451.2:n.1470+172G=
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