Canonical Allele Identifier: CA360485216

Gene: PCSK1

Linked Data

• gnomAD v4: 5-96429251-C-T
• MyVariant Identifiers: chr5:g.95764955C>T (hg19) ; chr5:g.96429251C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96429251C>T , CM000667.2:g.96429251C>T	GRCh38
NC_000005.9:g.95764955C>T , CM000667.1:g.95764955C>T	GRCh37
NC_000005.8:g.95790711C>T	NCBI36
NG_021161.1:g.9031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311106.8:c.247G>A MANE Select	ENSP00000308024.2:p.Ala83Thr
ENST00000311106.7:c.247G>A	ENSP00000308024.2:p.Ala83Thr
ENST00000508626.5:c.106G>A	ENSP00000421600.1:p.Ala36Thr
ENST00000509190.1:c.247G>A	ENSP00000427294.1:p.Ala83Thr
NM_000439.4:c.247G>A	NP_000430.3:p.Ala83Thr
NM_001177875.1:c.106G>A	NP_001171346.1:p.Ala36Thr
NR_130776.1:n.354+49599C>T
NM_000439.5:c.247G>A MANE Select	NP_000430.3:p.Ala83Thr
NM_001177875.2:c.106G>A	NP_001171346.1:p.Ala36Thr