Canonical Allele Identifier: CA367923004
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392570C>G , CM000669.2:g.83392570C>G GRCh38
NC_000007.13:g.83021886C>G , CM000669.1:g.83021886C>G GRCh37
NC_000007.12:g.82859822C>G NCBI36
NG_021242.1:g.261594G>C
NG_021242.2:g.261594G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1472G>C ENSP00000405052.1:p.Gly491Ala
ENST00000642232.1:c.1652G>C ENSP00000494064.1:p.Gly551Ala
ENST00000643230.2:c.1652G>C MANE Select ENSP00000496491.1:p.Gly551Ala
ENST00000643441.1:n.1637G>C
ENST00000307792.7:c.1652G>C ENSP00000303212.3:p.Gly551Ala
ENST00000427262.5:c.1472G>C ENSP00000405052.1:p.Gly491Ala
NM_001178129.1:c.1472G>C NP_001171600.1:p.Gly491Ala
NM_012431.2:c.1652G>C NP_036563.1:p.Gly551Ala
XM_011516715.1:c.1652G>C XP_011515017.1:p.Gly551Ala
NM_012431.3:c.1652G>C MANE Select NP_036563.1:p.Gly551Ala
NM_001178129.2:c.1472G>C NP_001171600.1:p.Gly491Ala