Canonical Allele Identifier: CA1565417022
Gene: PCSK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96426799T= , CM000667.2:g.96426799T= GRCh38
NC_000005.9:g.95762503T= , CM000667.1:g.95762503T= GRCh37
NC_000005.8:g.95788259T= NCBI36
NG_021161.1:g.11483A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311106.8:c.286-869A= MANE Select ENSP00000308024.2:n.286-869A=
ENST00000311106.7:c.286-869A= ENSP00000308024.2:n.286-869A=
ENST00000508626.5:c.145-869A= ENSP00000421600.1:n.145-869A=
ENST00000509190.1:c.286-869A= ENSP00000427294.1:n.286-869A=
NM_000439.4:c.286-869A= NP_000430.3:n.286-869A=
NM_001177875.1:c.145-869A= NP_001171346.1:n.145-869A=
NR_130776.1:n.354+47147T=
NM_000439.5:c.286-869A= MANE Select NP_000430.3:n.286-869A=
NM_001177875.2:c.145-869A= NP_001171346.1:n.145-869A=
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