Canonical Allele Identifier: CA122918541
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs77129335
gnomAD v2: 5-95751582-G-A
gnomAD v3: 5-96415878-G-A
gnomAD v4: 5-96415878-G-A
MyVariant Identifiers: chr5:g.95751582G>A (hg19) chr5:g.96415878G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96415878G>A , CM000667.2:g.96415878G>A GRCh38
NC_000005.9:g.95751582G>A , CM000667.1:g.95751582G>A GRCh37
NC_000005.8:g.95777338G>A NCBI36
NG_021161.1:g.22404C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.709+155C>T MANE Select ENSP00000308024.2:n.709+155C>T
ENST00000311106.7:c.709+155C>T ENSP00000308024.2:n.709+155C>T
ENST00000508626.5:c.568+155C>T ENSP00000421600.1:n.568+155C>T
NM_000439.4:c.709+155C>T NP_000430.3:n.709+155C>T
NM_001177875.1:c.568+155C>T NP_001171346.1:n.568+155C>T
NR_130776.1:n.354+36226G>A
NM_000439.5:c.709+155C>T MANE Select NP_000430.3:n.709+155C>T
NM_001177875.2:c.568+155C>T NP_001171346.1:n.568+155C>T
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