Canonical Allele Identifier: CA1565417014
Gene: PCSK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96426782G= , CM000667.2:g.96426782G= GRCh38
NC_000005.9:g.95762486G= , CM000667.1:g.95762486G= GRCh37
NC_000005.8:g.95788242G= NCBI36
NG_021161.1:g.11500C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.286-852C= MANE Select ENSP00000308024.2:n.286-852C=
ENST00000311106.7:c.286-852C= ENSP00000308024.2:n.286-852C=
ENST00000508626.5:c.145-852C= ENSP00000421600.1:n.145-852C=
ENST00000509190.1:c.286-852C= ENSP00000427294.1:n.286-852C=
NM_000439.4:c.286-852C= NP_000430.3:n.286-852C=
NM_001177875.1:c.145-852C= NP_001171346.1:n.145-852C=
NR_130776.1:n.354+47130G=
NM_000439.5:c.286-852C= MANE Select NP_000430.3:n.286-852C=
NM_001177875.2:c.145-852C= NP_001171346.1:n.145-852C=
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