Canonical Allele Identifier: CA367930212

Gene: SEMA3E

Linked Data

• MyVariant Identifiers: chr7:g.83036444G>T (hg19) ; chr7:g.83407128G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407128G>T , CM000669.2:g.83407128G>T	GRCh38
NC_000007.13:g.83036444G>T , CM000669.1:g.83036444G>T	GRCh37
NC_000007.12:g.82874380G>T	NCBI36
NG_021242.1:g.247036C>A
NG_021242.2:g.247036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.602C>A	ENSP00000405052.1:p.Ala201Glu
ENST00000642232.1:c.782C>A	ENSP00000494064.1:p.Ala261Glu
ENST00000643230.2:c.782C>A MANE Select	ENSP00000496491.1:p.Ala261Glu
ENST00000643441.1:n.767C>A
ENST00000307792.7:c.782C>A	ENSP00000303212.3:p.Ala261Glu
ENST00000427262.5:c.602C>A	ENSP00000405052.1:p.Ala201Glu
NM_001178129.1:c.602C>A	NP_001171600.1:p.Ala201Glu
NM_012431.2:c.782C>A	NP_036563.1:p.Ala261Glu
XM_011516715.1:c.782C>A	XP_011515017.1:p.Ala261Glu
NM_012431.3:c.782C>A MANE Select	NP_036563.1:p.Ala261Glu
NM_001178129.2:c.602C>A	NP_001171600.1:p.Ala201Glu