Canonical Allele Identifier: CA445498884
Gene: PCSK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.95764965A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429261A>T , CM000667.2:g.96429261A>T GRCh38
NC_000005.9:g.95764965A>T , CM000667.1:g.95764965A>T GRCh37
NC_000005.8:g.95790721A>T NCBI36
NG_021161.1:g.9021T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.237T>A MANE Select ENSP00000308024.2:p.Ser79=
ENST00000311106.7:c.237T>A ENSP00000308024.2:p.Ser79=
ENST00000508626.5:c.96T>A ENSP00000421600.1:p.Ser32=
ENST00000509190.1:c.237T>A ENSP00000427294.1:p.Ser79=
NM_000439.4:c.237T>A NP_000430.3:p.Ser79=
NM_001177875.1:c.96T>A NP_001171346.1:p.Ser32=
NR_130776.1:n.354+49609A>T
NM_000439.5:c.237T>A MANE Select NP_000430.3:p.Ser79=
NM_001177875.2:c.96T>A NP_001171346.1:p.Ser32=