Canonical Allele Identifier: CA445496770
Gene: PCSK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.95751815T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96416111T>G , CM000667.2:g.96416111T>G GRCh38
NC_000005.9:g.95751815T>G , CM000667.1:g.95751815T>G GRCh37
NC_000005.8:g.95777571T>G NCBI36
NG_021161.1:g.22171A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.631A>C MANE Select ENSP00000308024.2:p.Arg211=
ENST00000311106.7:c.631A>C ENSP00000308024.2:p.Arg211=
ENST00000508626.5:c.490A>C ENSP00000421600.1:p.Arg164=
NM_000439.4:c.631A>C NP_000430.3:p.Arg211=
NM_001177875.1:c.490A>C NP_001171346.1:p.Arg164=
NR_130776.1:n.354+36459T>G
NM_000439.5:c.631A>C MANE Select NP_000430.3:p.Arg211=
NM_001177875.2:c.490A>C NP_001171346.1:p.Arg164=