Canonical Allele Identifier: CA445719849
Gene: PCSK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.95728945A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96393241A>C , CM000667.2:g.96393241A>C GRCh38
NC_000005.9:g.95728945A>C , CM000667.1:g.95728945A>C GRCh37
NC_000005.8:g.95754701A>C NCBI36
NG_021161.1:g.45041T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.2022T>G MANE Select ENSP00000308024.2:p.Ala674=
ENST00000311106.7:c.2022T>G ENSP00000308024.2:p.Ala674=
ENST00000508626.5:c.1881T>G ENSP00000421600.1:p.Ala627=
ENST00000513085.1:n.1165T>G
NM_000439.4:c.2022T>G NP_000430.3:p.Ala674=
NM_001177875.1:c.1881T>G NP_001171346.1:p.Ala627=
NR_130776.1:n.354+13589A>C
NM_000439.5:c.2022T>G MANE Select NP_000430.3:p.Ala674=
NM_001177875.2:c.1881T>G NP_001171346.1:p.Ala627=