Canonical Allele Identifier: CA456133468

Gene: SEMA3E

Linked Data

• dbSNP Id: rs1454351864
• gnomAD v2: 7-83021939-T-C
• gnomAD v4: 7-83392623-T-C
• MyVariant Identifiers: chr7:g.83021939T>C (hg19) ; chr7:g.83392623T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392623T>C , CM000669.2:g.83392623T>C	GRCh38
NC_000007.13:g.83021939T>C , CM000669.1:g.83021939T>C	GRCh37
NC_000007.12:g.82859875T>C	NCBI36
NG_021242.1:g.261541A>G
NG_021242.2:g.261541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1419A>G	ENSP00000405052.1:p.Arg473=
ENST00000642232.1:c.1599A>G	ENSP00000494064.1:p.Arg533=
ENST00000643230.2:c.1599A>G MANE Select	ENSP00000496491.1:p.Arg533=
ENST00000643441.1:n.1584A>G
ENST00000307792.7:c.1599A>G	ENSP00000303212.3:p.Arg533=
ENST00000427262.5:c.1419A>G	ENSP00000405052.1:p.Arg473=
NM_001178129.1:c.1419A>G	NP_001171600.1:p.Arg473=
NM_012431.2:c.1599A>G	NP_036563.1:p.Arg533=
XM_011516715.1:c.1599A>G	XP_011515017.1:p.Arg533=
NM_012431.3:c.1599A>G MANE Select	NP_036563.1:p.Arg533=
NM_001178129.2:c.1419A>G	NP_001171600.1:p.Arg473=