Canonical Allele Identifier: CA15587570

Gene: PCSK5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.76150085C>T , CM000671.2:g.76150085C>T	GRCh38
NC_000009.11:g.78765001C>T , CM000671.1:g.78765001C>T	GRCh37
NC_000009.10:g.77954821C>T	NCBI36
NG_029445.1:g.264442C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376752.9:c.1313-6960C>T	ENSP00000365943.4:n.1313-6960C>T
ENST00000674117.1:c.1313-6960C>T MANE Select	ENSP00000500971.1:n.1313-6960C>T
ENST00000376752.8:c.1313-6960C>T	ENSP00000365943.4:n.1313-6960C>T
ENST00000376767.7:c.1313-6960C>T	ENSP00000365958.3:n.1313-6960C>T
ENST00000424854.6:c.332-6960C>T	ENSP00000411654.1:n.332-6960C>T
ENST00000545128.5:c.1313-6960C>T	ENSP00000446280.1:n.1313-6960C>T
NM_001190482.1:c.1313-6960C>T	NP_001177411.1:n.1313-6960C>T
NM_006200.5:c.1313-6960C>T	NP_006191.2:n.1313-6960C>T
NR_120409.1:n.1747-6960C>T
XM_005252039.2:c.1313-6960C>T	XP_005252096.1:n.1313-6960C>T
XM_011518769.1:c.1313-6960C>T	XP_011517071.1:n.1313-6960C>T
XM_011518770.1:c.-26-6960C>T	XP_011517072.1:n.-26-6960C>T
XR_929806.1:n.1894-6960C>T
XR_929807.1:n.1894-6960C>T
XM_005252039.4:c.1313-6960C>T	XP_005252096.1:n.1313-6960C>T
XM_011518769.3:c.1313-6960C>T	XP_011517071.1:n.1313-6960C>T
XM_011518770.2:c.-26-6960C>T	XP_011517072.1:n.-26-6960C>T
XM_017014800.1:c.2-6960C>T	XP_016870289.1:n.2-6960C>T
XR_929806.2:n.1849-6960C>T
XR_929807.2:n.1849-6960C>T
NM_001372043.1:c.1313-6960C>T MANE Select	NP_001358972.1:n.1313-6960C>T
NM_006200.6:c.1313-6960C>T	NP_006191.2:n.1313-6960C>T
NR_120409.2:n.1718-6960C>T
NM_001190482.2:c.1313-6960C>T	NP_001177411.1:n.1313-6960C>T