Canonical Allele Identifier: CA367922940
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392557T>A , CM000669.2:g.83392557T>A GRCh38
NC_000007.13:g.83021873T>A , CM000669.1:g.83021873T>A GRCh37
NC_000007.12:g.82859809T>A NCBI36
NG_021242.1:g.261607A>T
NG_021242.2:g.261607A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1485A>T ENSP00000405052.1:p.Lys495Asn
ENST00000642232.1:c.1665A>T ENSP00000494064.1:p.Lys555Asn
ENST00000643230.2:c.1665A>T MANE Select ENSP00000496491.1:p.Lys555Asn
ENST00000643441.1:n.1650A>T
ENST00000307792.7:c.1665A>T ENSP00000303212.3:p.Lys555Asn
ENST00000427262.5:c.1485A>T ENSP00000405052.1:p.Lys495Asn
NM_001178129.1:c.1485A>T NP_001171600.1:p.Lys495Asn
NM_012431.2:c.1665A>T NP_036563.1:p.Lys555Asn
XM_011516715.1:c.1665A>T XP_011515017.1:p.Lys555Asn
NM_012431.3:c.1665A>T MANE Select NP_036563.1:p.Lys555Asn
NM_001178129.2:c.1485A>T NP_001171600.1:p.Lys495Asn