Canonical Allele Identifier: CA417960716

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529233G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063560G>C , CM000663.2:g.55063560G>C	GRCh38
NC_000001.10:g.55529233G>C , CM000663.1:g.55529233G>C	GRCh37
NC_000001.9:g.55301821G>C	NCBI36
NG_009061.1:g.29014G>C , LRG_275:g.29014G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*395G>C	ENSP00000501161.2:n.*395G>C
ENST00000710286.1:c.2412G>C	ENSP00000518176.1:p.Ala804=
ENST00000673903.1:c.1680G>C	ENSP00000501257.1:p.Ala560=
ENST00000302118.5:c.2055G>C MANE Select	ENSP00000303208.5:p.Ala685=
ENST00000490692.1:n.2601G>C
NM_174936.3:c.2055G>C , LRG_275t1:c.2055G>C	NP_777596.2:p.Ala685=
NR_110451.1:n.1662G>C
XM_011541193.1:c.1176G>C	XP_011539495.1:p.Ala392=
NM_174936.4:c.2055G>C MANE Select	NP_777596.2:p.Ala685=
NR_110451.2:n.1662G>C