Canonical Allele Identifier: CA367930340
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407185T>C , CM000669.2:g.83407185T>C GRCh38
NC_000007.13:g.83036501T>C , CM000669.1:g.83036501T>C GRCh37
NC_000007.12:g.82874437T>C NCBI36
NG_021242.1:g.246979A>G
NG_021242.2:g.246979A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.545A>G ENSP00000405052.1:p.Asn182Ser
ENST00000642232.1:c.725A>G ENSP00000494064.1:p.Asn242Ser
ENST00000643230.2:c.725A>G MANE Select ENSP00000496491.1:p.Asn242Ser
ENST00000643441.1:n.710A>G
ENST00000644381.1:n.288A>G
ENST00000307792.7:c.725A>G ENSP00000303212.3:p.Asn242Ser
ENST00000427262.5:c.545A>G ENSP00000405052.1:p.Asn182Ser
NM_001178129.1:c.545A>G NP_001171600.1:p.Asn182Ser
NM_012431.2:c.725A>G NP_036563.1:p.Asn242Ser
XM_011516715.1:c.725A>G XP_011515017.1:p.Asn242Ser
NM_012431.3:c.725A>G MANE Select NP_036563.1:p.Asn242Ser
NM_001178129.2:c.545A>G NP_001171600.1:p.Asn182Ser