Canonical Allele Identifier: CA456135983

Gene: SEMA3E

Linked Data

• ClinVar Variation Id: 2037928
• ClinVar RCV Id: RCV002890335
• dbSNP Id: rs1399787086
• gnomAD v2: 7-83036518-A-G
• gnomAD v3: 7-83407202-A-G
• gnomAD v4: 7-83407202-A-G
• MyVariant Identifiers: chr7:g.83036518A>G (hg19) ; chr7:g.83407202A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407202A>G , CM000669.2:g.83407202A>G	GRCh38
NC_000007.13:g.83036518A>G , CM000669.1:g.83036518A>G	GRCh37
NC_000007.12:g.82874454A>G	NCBI36
NG_021242.1:g.246962T>C
NG_021242.2:g.246962T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.528T>C	ENSP00000405052.1:p.Asn176=
ENST00000642232.1:c.708T>C	ENSP00000494064.1:p.Asn236=
ENST00000643230.2:c.708T>C MANE Select	ENSP00000496491.1:p.Asn236=
ENST00000643441.1:n.693T>C
ENST00000644381.1:n.271T>C
ENST00000307792.7:c.708T>C	ENSP00000303212.3:p.Asn236=
ENST00000427262.5:c.528T>C	ENSP00000405052.1:p.Asn176=
NM_001178129.1:c.528T>C	NP_001171600.1:p.Asn176=
NM_012431.2:c.708T>C	NP_036563.1:p.Asn236=
XM_011516715.1:c.708T>C	XP_011515017.1:p.Asn236=
NM_012431.3:c.708T>C MANE Select	NP_036563.1:p.Asn236=
NM_001178129.2:c.528T>C	NP_001171600.1:p.Asn176=