Canonical Allele Identifier: CA415101869

Gene: PLXNB3

Linked Data

• COSMIC: COSM3559522 ; COSM3559523 ; COSM3559524
• MyVariant Identifiers: chrX:g.153035694C>T (hg19) ; chrX:g.153770239C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770239C>T , CM000685.2:g.153770239C>T	GRCh38
NC_000023.10:g.153035694C>T , CM000685.1:g.153035694C>T	GRCh37
NC_000023.9:g.152688888C>T	NCBI36
NG_013255.1:g.11044C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361971.10:c.1777C>T MANE Select	ENSP00000355378.5:p.Pro593Ser
ENST00000361971.9:c.1777C>T	ENSP00000355378.5:p.Pro593Ser
ENST00000538966.5:c.1846C>T	ENSP00000442736.1:p.Pro616Ser
NM_001163257.1:c.1846C>T	NP_001156729.1:p.Pro616Ser
NM_005393.2:c.1777C>T	NP_005384.2:p.Pro593Ser
NM_005393.3:c.1777C>T MANE Select	NP_005384.2:p.Pro593Ser
NM_001163257.2:c.1846C>T	NP_001156729.1:p.Pro616Ser