Canonical Allele Identifier: CA456133475
Gene: SEMA3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.83021945C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392629C>T , CM000669.2:g.83392629C>T GRCh38
NC_000007.13:g.83021945C>T , CM000669.1:g.83021945C>T GRCh37
NC_000007.12:g.82859881C>T NCBI36
NG_021242.1:g.261535G>A
NG_021242.2:g.261535G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.1413G>A ENSP00000405052.1:p.Leu471=
ENST00000642232.1:c.1593G>A ENSP00000494064.1:p.Leu531=
ENST00000643230.2:c.1593G>A MANE Select ENSP00000496491.1:p.Leu531=
ENST00000643441.1:n.1578G>A
ENST00000307792.7:c.1593G>A ENSP00000303212.3:p.Leu531=
ENST00000427262.5:c.1413G>A ENSP00000405052.1:p.Leu471=
NM_001178129.1:c.1413G>A NP_001171600.1:p.Leu471=
NM_012431.2:c.1593G>A NP_036563.1:p.Leu531=
XM_011516715.1:c.1593G>A XP_011515017.1:p.Leu531=
NM_012431.3:c.1593G>A MANE Select NP_036563.1:p.Leu531=
NM_001178129.2:c.1413G>A NP_001171600.1:p.Leu471=