Canonical Allele Identifier: CA456135744

Gene: SEMA3E

Linked Data

• dbSNP Id: rs1387707155
• gnomAD v2: 7-83036452-A-G
• gnomAD v4: 7-83407136-A-G
• MyVariant Identifiers: chr7:g.83036452A>G (hg19) ; chr7:g.83407136A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407136A>G , CM000669.2:g.83407136A>G	GRCh38
NC_000007.13:g.83036452A>G , CM000669.1:g.83036452A>G	GRCh37
NC_000007.12:g.82874388A>G	NCBI36
NG_021242.1:g.247028T>C
NG_021242.2:g.247028T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.594T>C	ENSP00000405052.1:p.Asn198=
ENST00000642232.1:c.774T>C	ENSP00000494064.1:p.Asn258=
ENST00000643230.2:c.774T>C MANE Select	ENSP00000496491.1:p.Asn258=
ENST00000643441.1:n.759T>C
ENST00000307792.7:c.774T>C	ENSP00000303212.3:p.Asn258=
ENST00000427262.5:c.594T>C	ENSP00000405052.1:p.Asn198=
NM_001178129.1:c.594T>C	NP_001171600.1:p.Asn198=
NM_012431.2:c.774T>C	NP_036563.1:p.Asn258=
XM_011516715.1:c.774T>C	XP_011515017.1:p.Asn258=
NM_012431.3:c.774T>C MANE Select	NP_036563.1:p.Asn258=
NM_001178129.2:c.594T>C	NP_001171600.1:p.Asn198=