Canonical Allele Identifier: CA1565418252
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1228396418

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429592C>G , CM000667.2:g.96429592C>G GRCh38
NC_000005.9:g.95765296C>G , CM000667.1:g.95765296C>G GRCh37
NC_000005.8:g.95791052C>G NCBI36
NG_021161.1:g.8690G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-275G>C MANE Select ENSP00000308024.2:n.181-275G>C
ENST00000311106.7:c.181-275G>C ENSP00000308024.2:n.181-275G>C
ENST00000508626.5:c.40-275G>C ENSP00000421600.1:n.40-275G>C
ENST00000509190.1:c.181-275G>C ENSP00000427294.1:n.181-275G>C
NM_000439.4:c.181-275G>C NP_000430.3:n.181-275G>C
NM_001177875.1:c.40-275G>C NP_001171346.1:n.40-275G>C
NR_130776.1:n.354+49940C>G
NM_000439.5:c.181-275G>C MANE Select NP_000430.3:n.181-275G>C
NM_001177875.2:c.40-275G>C NP_001171346.1:n.40-275G>C