Canonical Allele Identifier: CA456133542

Gene: SEMA3E

Linked Data

• MyVariant Identifiers: chr7:g.83022029C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392713C>G , CM000669.2:g.83392713C>G	GRCh38
NC_000007.13:g.83022029C>G , CM000669.1:g.83022029C>G	GRCh37
NC_000007.12:g.82859965C>G	NCBI36
NG_021242.1:g.261451G>C
NG_021242.2:g.261451G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1329G>C	ENSP00000405052.1:p.Leu443=
ENST00000642232.1:c.1509G>C	ENSP00000494064.1:p.Leu503=
ENST00000643230.2:c.1509G>C MANE Select	ENSP00000496491.1:p.Leu503=
ENST00000643441.1:n.1494G>C
ENST00000307792.7:c.1509G>C	ENSP00000303212.3:p.Leu503=
ENST00000427262.5:c.1329G>C	ENSP00000405052.1:p.Leu443=
NM_001178129.1:c.1329G>C	NP_001171600.1:p.Leu443=
NM_012431.2:c.1509G>C	NP_036563.1:p.Leu503=
XM_011516715.1:c.1509G>C	XP_011515017.1:p.Leu503=
NM_012431.3:c.1509G>C MANE Select	NP_036563.1:p.Leu503=
NM_001178129.2:c.1329G>C	NP_001171600.1:p.Leu443=