Canonical Allele Identifier: CA1856680008
Gene: PCSK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.76180343T= , CM000671.2:g.76180343T= GRCh38
NC_000009.11:g.78795259T= , CM000671.1:g.78795259T= GRCh37
NC_000009.10:g.77985079T= NCBI36
NG_029445.1:g.294700T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376752.9:c.2003+645T= ENSP00000365943.4:n.2003+645T=
ENST00000674117.1:c.2003+645T= MANE Select ENSP00000500971.1:n.2003+645T=
ENST00000376752.8:c.2003+645T= ENSP00000365943.4:n.2003+645T=
ENST00000424854.6:c.1022+645T= ENSP00000411654.1:n.1022+645T=
ENST00000545128.5:c.2003+645T= ENSP00000446280.1:n.2003+645T=
NM_001190482.1:c.2003+645T= NP_001177411.1:n.2003+645T=
NM_006200.5:c.2003+645T= NP_006191.2:n.2003+645T=
NR_120409.1:n.2437+645T=
XM_005252039.2:c.2003+645T= XP_005252096.1:n.2003+645T=
XM_011518769.1:c.2003+645T= XP_011517071.1:n.2003+645T=
XM_011518770.1:c.665+645T= XP_011517072.1:n.665+645T=
XR_929806.1:n.2584+645T=
XR_929807.1:n.2584+645T=
XM_005252039.4:c.2003+645T= XP_005252096.1:n.2003+645T=
XM_011518769.3:c.2003+645T= XP_011517071.1:n.2003+645T=
XM_011518770.2:c.665+645T= XP_011517072.1:n.665+645T=
XM_017014800.1:c.692+645T= XP_016870289.1:n.692+645T=
XR_929806.2:n.2539+645T=
XR_929807.2:n.2539+645T=
NM_001372043.1:c.2003+645T= MANE Select NP_001358972.1:n.2003+645T=
NM_006200.6:c.2003+645T= NP_006191.2:n.2003+645T=
NR_120409.2:n.2408+645T=
NM_001190482.2:c.2003+645T= NP_001177411.1:n.2003+645T=