Canonical Allele Identifier: CA122935562
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs577664084
gnomAD v3: 5-96429094-C-T
gnomAD v4: 5-96429094-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429094C>T , CM000667.2:g.96429094C>T GRCh38
NC_000005.9:g.95764798C>T , CM000667.1:g.95764798C>T GRCh37
NC_000005.8:g.95790554C>T NCBI36
NG_021161.1:g.9188G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.285+119G>A MANE Select ENSP00000308024.2:n.285+119G>A
ENST00000311106.7:c.285+119G>A ENSP00000308024.2:n.285+119G>A
ENST00000508626.5:c.144+119G>A ENSP00000421600.1:n.144+119G>A
ENST00000509190.1:c.285+119G>A ENSP00000427294.1:n.285+119G>A
NM_000439.4:c.285+119G>A NP_000430.3:n.285+119G>A
NM_001177875.1:c.144+119G>A NP_001171346.1:n.144+119G>A
NR_130776.1:n.354+49442C>T
NM_000439.5:c.285+119G>A MANE Select NP_000430.3:n.285+119G>A
NM_001177875.2:c.144+119G>A NP_001171346.1:n.144+119G>A