Canonical Allele Identifier: CA367930207
Gene: SEMA3E HGNC NCBI

Linked Data

gnomAD v4: 7-83407126-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407126T>A , CM000669.2:g.83407126T>A GRCh38
NC_000007.13:g.83036442T>A , CM000669.1:g.83036442T>A GRCh37
NC_000007.12:g.82874378T>A NCBI36
NG_021242.1:g.247038A>T
NG_021242.2:g.247038A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.604A>T ENSP00000405052.1:p.Ile202Phe
ENST00000642232.1:c.784A>T ENSP00000494064.1:p.Ile262Phe
ENST00000643230.2:c.784A>T MANE Select ENSP00000496491.1:p.Ile262Phe
ENST00000643441.1:n.769A>T
ENST00000307792.7:c.784A>T ENSP00000303212.3:p.Ile262Phe
ENST00000427262.5:c.604A>T ENSP00000405052.1:p.Ile202Phe
NM_001178129.1:c.604A>T NP_001171600.1:p.Ile202Phe
NM_012431.2:c.784A>T NP_036563.1:p.Ile262Phe
XM_011516715.1:c.784A>T XP_011515017.1:p.Ile262Phe
NM_012431.3:c.784A>T MANE Select NP_036563.1:p.Ile262Phe
NM_001178129.2:c.604A>T NP_001171600.1:p.Ile202Phe