Canonical Allele Identifier: CA1565418257
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1761428207

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429602_96429603insCT , CM000667.2:g.96429602_96429603insCT GRCh38
NC_000005.9:g.95765306_95765307insCT , CM000667.1:g.95765306_95765307insCT GRCh37
NC_000005.8:g.95791062_95791063insCT NCBI36
NG_021161.1:g.8679_8680insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-286_181-285insAG MANE Select ENSP00000308024.2:n.181-286_181-285insAG
ENST00000311106.7:c.181-286_181-285insAG ENSP00000308024.2:n.181-286_181-285insAG
ENST00000508626.5:c.40-286_40-285insAG ENSP00000421600.1:n.40-286_40-285insAG
ENST00000509190.1:c.181-286_181-285insAG ENSP00000427294.1:n.181-286_181-285insAG
NM_000439.4:c.181-286_181-285insAG NP_000430.3:n.181-286_181-285insAG
NM_001177875.1:c.40-286_40-285insAG NP_001171346.1:n.40-286_40-285insAG
NR_130776.1:n.354+49950_354+49951insCT
NM_000439.5:c.181-286_181-285insAG MANE Select NP_000430.3:n.181-286_181-285insAG
NM_001177875.2:c.40-286_40-285insAG NP_001171346.1:n.40-286_40-285insAG