Canonical Allele Identifier: CA2838627722

Gene: PLXNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770210dup , CM000685.2:g.153770210dup	GRCh38
NC_000023.10:g.153035665dup , CM000685.1:g.153035665dup	GRCh37
NC_000023.9:g.152688859dup	NCBI36
NG_013255.1:g.11015dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1748dup MANE Select	ENSP00000355378.5:p.Pro584SerfsTer8
ENST00000361971.9:c.1748dup	ENSP00000355378.5:p.Pro584SerfsTer8
ENST00000538966.5:c.1817dup	ENSP00000442736.1:p.Pro607SerfsTer8
NM_001163257.1:c.1817dup	NP_001156729.1:p.Pro607SerfsTer8
NM_005393.2:c.1748dup	NP_005384.2:p.Pro584SerfsTer8
NM_005393.3:c.1748dup MANE Select	NP_005384.2:p.Pro584SerfsTer8
NM_001163257.2:c.1817dup	NP_001156729.1:p.Pro607SerfsTer8