Canonical Allele Identifier: CA122918532
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs74418748
gnomAD v2: 5-95751533-T-A
gnomAD v3: 5-96415829-T-A
gnomAD v4: 5-96415829-T-A
MyVariant Identifiers: chr5:g.95751533T>A (hg19) chr5:g.96415829T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96415829T>A , CM000667.2:g.96415829T>A GRCh38
NC_000005.9:g.95751533T>A , CM000667.1:g.95751533T>A GRCh37
NC_000005.8:g.95777289T>A NCBI36
NG_021161.1:g.22453A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.709+204A>T MANE Select ENSP00000308024.2:n.709+204A>T
ENST00000311106.7:c.709+204A>T ENSP00000308024.2:n.709+204A>T
ENST00000508626.5:c.568+204A>T ENSP00000421600.1:n.568+204A>T
NM_000439.4:c.709+204A>T NP_000430.3:n.709+204A>T
NM_001177875.1:c.568+204A>T NP_001171346.1:n.568+204A>T
NR_130776.1:n.354+36177T>A
NM_000439.5:c.709+204A>T MANE Select NP_000430.3:n.709+204A>T
NM_001177875.2:c.568+204A>T NP_001171346.1:n.568+204A>T
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