Canonical Allele Identifier: CA367936071
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83469244G>T , CM000669.2:g.83469244G>T GRCh38
NC_000007.13:g.83098560G>T , CM000669.1:g.83098560G>T GRCh37
NC_000007.12:g.82936496G>T NCBI36
NG_021242.1:g.184920C>A
NG_021242.2:g.184920C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.155C>A ENSP00000405052.1:p.Ala52Glu
ENST00000642232.1:c.335C>A ENSP00000494064.1:p.Ala112Glu
ENST00000643230.2:c.335C>A MANE Select ENSP00000496491.1:p.Ala112Glu
ENST00000643441.1:n.320C>A
ENST00000307792.7:c.335C>A ENSP00000303212.3:p.Ala112Glu
ENST00000427262.5:c.155C>A ENSP00000405052.1:p.Ala52Glu
ENST00000442159.3:c.155C>A ENSP00000412867.3:p.Ala52Glu
NM_001178129.1:c.155C>A NP_001171600.1:p.Ala52Glu
NM_012431.2:c.335C>A NP_036563.1:p.Ala112Glu
XM_011516715.1:c.335C>A XP_011515017.1:p.Ala112Glu
NM_012431.3:c.335C>A MANE Select NP_036563.1:p.Ala112Glu
NM_001178129.2:c.155C>A NP_001171600.1:p.Ala52Glu