Canonical Allele Identifier: CA1079028099
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1761427856
gnomAD v3: 5-96429591-T-G
gnomAD v4: 5-96429591-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429591T>G , CM000667.2:g.96429591T>G GRCh38
NC_000005.9:g.95765295T>G , CM000667.1:g.95765295T>G GRCh37
NC_000005.8:g.95791051T>G NCBI36
NG_021161.1:g.8691A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-274A>C MANE Select ENSP00000308024.2:n.181-274A>C
ENST00000311106.7:c.181-274A>C ENSP00000308024.2:n.181-274A>C
ENST00000508626.5:c.40-274A>C ENSP00000421600.1:n.40-274A>C
ENST00000509190.1:c.181-274A>C ENSP00000427294.1:n.181-274A>C
NM_000439.4:c.181-274A>C NP_000430.3:n.181-274A>C
NM_001177875.1:c.40-274A>C NP_001171346.1:n.40-274A>C
NR_130776.1:n.354+49939T>G
NM_000439.5:c.181-274A>C MANE Select NP_000430.3:n.181-274A>C
NM_001177875.2:c.40-274A>C NP_001171346.1:n.40-274A>C
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