Canonical Allele Identifier: CA194599205

Gene: PCSK5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.75986163A>G , CM000671.2:g.75986163A>G	GRCh38
NC_000009.11:g.78601079A>G , CM000671.1:g.78601079A>G	GRCh37
NC_000009.10:g.77790899A>G	NCBI36
NG_029445.1:g.100520A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376752.9:c.329A>G	ENSP00000365943.4:p.Lys110Arg
ENST00000674117.1:c.329A>G MANE Select	ENSP00000500971.1:p.Lys110Arg
ENST00000376752.8:c.329A>G	ENSP00000365943.4:p.Lys110Arg
ENST00000376767.7:c.329A>G	ENSP00000365958.3:p.Lys110Arg
ENST00000545128.5:c.329A>G	ENSP00000446280.1:p.Lys110Arg
NM_001190482.1:c.329A>G	NP_001177411.1:p.Lys110Arg
NM_006200.5:c.329A>G	NP_006191.2:p.Lys110Arg
NR_120409.1:n.867A>G
XM_005252039.2:c.329A>G	XP_005252096.1:p.Lys110Arg
XM_011518769.1:c.329A>G	XP_011517071.1:p.Lys110Arg
XR_929806.1:n.910A>G
XR_929807.1:n.910A>G
XM_005252039.4:c.329A>G	XP_005252096.1:p.Lys110Arg
XM_011518769.3:c.329A>G	XP_011517071.1:p.Lys110Arg
XR_929806.2:n.865A>G
XR_929807.2:n.865A>G
NM_001372043.1:c.329A>G MANE Select	NP_001358972.1:p.Lys110Arg
NM_006200.6:c.329A>G	NP_006191.2:p.Lys110Arg
NR_120409.2:n.838A>G
NM_001190482.2:c.329A>G	NP_001177411.1:p.Lys110Arg