Canonical Allele Identifier: CA873290849

Gene: PLXNB3

Linked Data

• dbSNP Id: rs1191353754
• gnomAD v3: X-153770261-TGGG-T
• gnomAD v4: X-153770261-TGGG-T
• MyVariant Identifiers: chrX:g.153770262_153770264del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153770263_153770265del , CM000685.2:g.153770263_153770265del	GRCh38
NC_000023.10:g.153035718_153035720del , CM000685.1:g.153035718_153035720del	GRCh37
NC_000023.9:g.152688912_152688914del	NCBI36
NG_013255.1:g.11068_11070del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361971.10:c.1786+15_1786+17del MANE Select	ENSP00000355378.5:n.1786+15_1786+17del
ENST00000361971.9:c.1786+15_1786+17del	ENSP00000355378.5:n.1786+15_1786+17del
ENST00000538966.5:c.1855+15_1855+17del	ENSP00000442736.1:n.1855+15_1855+17del
NM_001163257.1:c.1855+15_1855+17del	NP_001156729.1:n.1855+15_1855+17del
NM_005393.2:c.1786+15_1786+17del	NP_005384.2:n.1786+15_1786+17del
NM_005393.3:c.1786+15_1786+17del MANE Select	NP_005384.2:n.1786+15_1786+17del
NM_001163257.2:c.1855+15_1855+17del	NP_001156729.1:n.1855+15_1855+17del