Canonical Allele Identifier: CA445498899
Gene: PCSK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.95765001G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429297G>A , CM000667.2:g.96429297G>A GRCh38
NC_000005.9:g.95765001G>A , CM000667.1:g.95765001G>A GRCh37
NC_000005.8:g.95790757G>A NCBI36
NG_021161.1:g.8985C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.201C>T MANE Select ENSP00000308024.2:p.His67=
ENST00000311106.7:c.201C>T ENSP00000308024.2:p.His67=
ENST00000508626.5:c.60C>T ENSP00000421600.1:p.His20=
ENST00000509190.1:c.201C>T ENSP00000427294.1:p.His67=
NM_000439.4:c.201C>T NP_000430.3:p.His67=
NM_001177875.1:c.60C>T NP_001171346.1:p.His20=
NR_130776.1:n.354+49645G>A
NM_000439.5:c.201C>T MANE Select NP_000430.3:p.His67=
NM_001177875.2:c.60C>T NP_001171346.1:p.His20=