Canonical Allele Identifier: CA340480473
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55061527-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061527G>T , CM000663.2:g.55061527G>T GRCh38
NC_000001.10:g.55527200G>T , CM000663.1:g.55527200G>T GRCh37
NC_000001.9:g.55299788G>T NCBI36
NG_009061.1:g.26981G>T , LRG_275:g.26981G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*174G>T ENSP00000501161.2:n.*174G>T
ENST00000710286.1:c.2191G>T ENSP00000518176.1:p.Glu731Ter
ENST00000673903.1:c.1459G>T ENSP00000501257.1:p.Glu487Ter
ENST00000673913.1:c.684G>T ENSP00000501161.1:n.684G>T
ENST00000302118.5:c.1834G>T MANE Select ENSP00000303208.5:p.Glu612Ter
ENST00000490692.1:n.2380G>T
NM_174936.3:c.1834G>T , LRG_275t1:c.1834G>T NP_777596.2:p.Glu612Ter
NR_110451.1:n.1441G>T
XM_011541193.1:c.955G>T XP_011539495.1:p.Glu319Ter
NM_174936.4:c.1834G>T MANE Select NP_777596.2:p.Glu612Ter
NR_110451.2:n.1441G>T