Canonical Allele Identifier: CA3350567
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs776050328
gnomAD v2: 5-95765058-C-T
gnomAD v4: 5-96429354-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429354C>T , CM000667.2:g.96429354C>T GRCh38
NC_000005.9:g.95765058C>T , CM000667.1:g.95765058C>T GRCh37
NC_000005.8:g.95790814C>T NCBI36
NG_021161.1:g.8928G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-37G>A MANE Select ENSP00000308024.2:n.181-37G>A
ENST00000311106.7:c.181-37G>A ENSP00000308024.2:n.181-37G>A
ENST00000508626.5:c.40-37G>A ENSP00000421600.1:n.40-37G>A
ENST00000509190.1:c.181-37G>A ENSP00000427294.1:n.181-37G>A
NM_000439.4:c.181-37G>A NP_000430.3:n.181-37G>A
NM_001177875.1:c.40-37G>A NP_001171346.1:n.40-37G>A
NR_130776.1:n.354+49702C>T
NM_000439.5:c.181-37G>A MANE Select NP_000430.3:n.181-37G>A
NM_001177875.2:c.40-37G>A NP_001171346.1:n.40-37G>A