Canonical Allele Identifier: CA122936222
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs556616015
gnomAD v3: 5-96429605-C-T
gnomAD v4: 5-96429605-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429605C>T , CM000667.2:g.96429605C>T GRCh38
NC_000005.9:g.95765309C>T , CM000667.1:g.95765309C>T GRCh37
NC_000005.8:g.95791065C>T NCBI36
NG_021161.1:g.8677G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-288G>A MANE Select ENSP00000308024.2:n.181-288G>A
ENST00000311106.7:c.181-288G>A ENSP00000308024.2:n.181-288G>A
ENST00000508626.5:c.40-288G>A ENSP00000421600.1:n.40-288G>A
ENST00000509190.1:c.181-288G>A ENSP00000427294.1:n.181-288G>A
NM_000439.4:c.181-288G>A NP_000430.3:n.181-288G>A
NM_001177875.1:c.40-288G>A NP_001171346.1:n.40-288G>A
NR_130776.1:n.354+49953C>T
NM_000439.5:c.181-288G>A MANE Select NP_000430.3:n.181-288G>A
NM_001177875.2:c.40-288G>A NP_001171346.1:n.40-288G>A