Canonical Allele Identifier: CA417960551

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55527172T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061499T>C , CM000663.2:g.55061499T>C	GRCh38
NC_000001.10:g.55527172T>C , CM000663.1:g.55527172T>C	GRCh37
NC_000001.9:g.55299760T>C	NCBI36
NG_009061.1:g.26953T>C , LRG_275:g.26953T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*146T>C	ENSP00000501161.2:n.*146T>C
ENST00000710286.1:c.2163T>C	ENSP00000518176.1:p.His721=
ENST00000673903.1:c.1431T>C	ENSP00000501257.1:p.His477=
ENST00000673913.1:c.656T>C	ENSP00000501161.1:n.656T>C
ENST00000302118.5:c.1806T>C MANE Select	ENSP00000303208.5:p.His602=
ENST00000490692.1:n.2352T>C
NM_174936.3:c.1806T>C , LRG_275t1:c.1806T>C	NP_777596.2:p.His602=
NR_110451.1:n.1413T>C
XM_011541193.1:c.927T>C	XP_011539495.1:p.His309=
NM_174936.4:c.1806T>C MANE Select	NP_777596.2:p.His602=
NR_110451.2:n.1413T>C