Canonical Allele Identifier: CA14643634

Gene: PLAUR

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43668738A>C , CM000681.2:g.43668738A>C	GRCh38
NC_000019.9:g.44172890A>C , CM000681.1:g.44172890A>C	GRCh37
NC_000019.8:g.48864730A>C	NCBI36
NG_032898.1:g.6609T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340093.8:c.56-1047T>G MANE Select	ENSP00000339328.3:n.56-1047T>G
ENST00000221264.8:c.56-1047T>G	ENSP00000221264.3:n.56-1047T>G
ENST00000339082.7:c.56-1047T>G	ENSP00000342049.2:n.56-1047T>G
ENST00000340093.7:c.56-1047T>G	ENSP00000339328.3:n.56-1047T>G
ENST00000597107.1:c.55+1328T>G	ENSP00000471307.1:n.55+1328T>G
ENST00000598875.1:n.103-1047T>G
ENST00000601723.5:c.56-1047T>G	ENSP00000471881.1:n.56-1047T>G
ENST00000601876.1:n.104-1047T>G
NM_001005376.2:c.56-1047T>G	NP_001005376.1:n.56-1047T>G
NM_001005377.2:c.56-1047T>G	NP_001005377.1:n.56-1047T>G
NM_001301037.1:c.56-1047T>G	NP_001287966.1:n.56-1047T>G
NM_002659.3:c.56-1047T>G	NP_002650.1:n.56-1047T>G
XM_005258990.3:c.56-1047T>G	XP_005259047.1:n.56-1047T>G
XM_011527027.1:c.56-1047T>G	XP_011525329.1:n.56-1047T>G
XM_011527028.1:c.56-1047T>G	XP_011525330.1:n.56-1047T>G
XM_011527029.1:c.56-1047T>G	XP_011525331.1:n.56-1047T>G
XM_011527030.1:c.56-1047T>G	XP_011525332.1:n.56-1047T>G
XM_011527031.1:c.56-1047T>G	XP_011525333.1:n.56-1047T>G
XM_005258990.5:c.56-1047T>G	XP_005259047.1:n.56-1047T>G
XM_011527027.2:c.56-1047T>G	XP_011525329.1:n.56-1047T>G
XM_011527028.3:c.56-1047T>G	XP_011525330.1:n.56-1047T>G
XM_011527029.2:c.56-1047T>G	XP_011525331.1:n.56-1047T>G
XM_011527030.2:c.56-1047T>G	XP_011525332.1:n.56-1047T>G
XM_011527031.3:c.56-1047T>G	XP_011525333.1:n.56-1047T>G
NM_002659.4:c.56-1047T>G MANE Select	NP_002650.1:n.56-1047T>G
NM_001005377.3:c.56-1047T>G	NP_001005377.1:n.56-1047T>G
NM_001301037.2:c.56-1047T>G	NP_001287966.1:n.56-1047T>G
NM_001005376.3:c.56-1047T>G	NP_001005376.1:n.56-1047T>G