Canonical Allele Identifier: CA2574381354
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061597G>C , CM000663.2:g.55061597G>C GRCh38
NC_000001.10:g.55527270G>C , CM000663.1:g.55527270G>C GRCh37
NC_000001.9:g.55299858G>C NCBI36
NG_009061.1:g.27051G>C , LRG_275:g.27051G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+41G>C ENSP00000501161.2:n.*203+41G>C
ENST00000710286.1:c.2220+41G>C ENSP00000518176.1:n.2220+41G>C
ENST00000673903.1:c.1488+41G>C ENSP00000501257.1:n.1488+41G>C
ENST00000673913.1:c.713+41G>C ENSP00000501161.1:n.713+41G>C
ENST00000302118.5:c.1863+41G>C MANE Select ENSP00000303208.5:n.1863+41G>C
ENST00000490692.1:n.2409+41G>C
NM_174936.3:c.1863+41G>C , LRG_275t1:c.1863+41G>C NP_777596.2:n.1863+41G>C
NR_110451.1:n.1470+41G>C
XM_011541193.1:c.984+41G>C XP_011539495.1:n.984+41G>C
NM_174936.4:c.1863+41G>C MANE Select NP_777596.2:n.1863+41G>C
NR_110451.2:n.1470+41G>C