Canonical Allele Identifier: CA1856713358

Gene: PCSK5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.76254665G= , CM000671.2:g.76254665G=	GRCh38
NC_000009.11:g.78869581G= , CM000671.1:g.78869581G=	GRCh37
NC_000009.10:g.78059401G=	NCBI36
NG_029445.1:g.369022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674117.1:c.3142+13981G= MANE Select	ENSP00000500971.1:n.3142+13981G=
ENST00000424854.6:c.2161+13981G=	ENSP00000411654.1:n.2161+13981G=
ENST00000545128.5:c.3142+13981G=	ENSP00000446280.1:n.3142+13981G=
NM_001190482.1:c.3142+13981G=	NP_001177411.1:n.3142+13981G=
XM_005252039.2:c.3142+13981G=	XP_005252096.1:n.3142+13981G=
XM_011518769.1:c.3142+13981G=	XP_011517071.1:n.3142+13981G=
XM_011518770.1:c.1804+13981G=	XP_011517072.1:n.1804+13981G=
XM_005252039.4:c.3142+13981G=	XP_005252096.1:n.3142+13981G=
XM_011518769.3:c.3142+13981G=	XP_011517071.1:n.3142+13981G=
XM_011518770.2:c.1804+13981G=	XP_011517072.1:n.1804+13981G=
XM_017014800.1:c.1831+13981G=	XP_016870289.1:n.1831+13981G=
NM_001372043.1:c.3142+13981G= MANE Select	NP_001358972.1:n.3142+13981G=
NM_001190482.2:c.3142+13981G=	NP_001177411.1:n.3142+13981G=