Canonical Allele Identifier: CA3350538
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs745911545
gnomAD v2: 5-95764888-T-G
gnomAD v4: 5-96429184-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429184T>G , CM000667.2:g.96429184T>G GRCh38
NC_000005.9:g.95764888T>G , CM000667.1:g.95764888T>G GRCh37
NC_000005.8:g.95790644T>G NCBI36
NG_021161.1:g.9098A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311106.8:c.285+29A>C MANE Select ENSP00000308024.2:n.285+29A>C
ENST00000311106.7:c.285+29A>C ENSP00000308024.2:n.285+29A>C
ENST00000508626.5:c.144+29A>C ENSP00000421600.1:n.144+29A>C
ENST00000509190.1:c.285+29A>C ENSP00000427294.1:n.285+29A>C
NM_000439.4:c.285+29A>C NP_000430.3:n.285+29A>C
NM_001177875.1:c.144+29A>C NP_001171346.1:n.144+29A>C
NR_130776.1:n.354+49532T>G
NM_000439.5:c.285+29A>C MANE Select NP_000430.3:n.285+29A>C
NM_001177875.2:c.144+29A>C NP_001171346.1:n.144+29A>C