Canonical Allele Identifier: CA122933468
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs997485358

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96426816A>C , CM000667.2:g.96426816A>C GRCh38
NC_000005.9:g.95762520A>C , CM000667.1:g.95762520A>C GRCh37
NC_000005.8:g.95788276A>C NCBI36
NG_021161.1:g.11466T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.286-886T>G MANE Select ENSP00000308024.2:n.286-886T>G
ENST00000311106.7:c.286-886T>G ENSP00000308024.2:n.286-886T>G
ENST00000508626.5:c.145-886T>G ENSP00000421600.1:n.145-886T>G
ENST00000509190.1:c.286-886T>G ENSP00000427294.1:n.286-886T>G
NM_000439.4:c.286-886T>G NP_000430.3:n.286-886T>G
NM_001177875.1:c.145-886T>G NP_001171346.1:n.145-886T>G
NR_130776.1:n.354+47164A>C
NM_000439.5:c.286-886T>G MANE Select NP_000430.3:n.286-886T>G
NM_001177875.2:c.145-886T>G NP_001171346.1:n.145-886T>G