Canonical Allele Identifier: CA2578928272
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407093T>G , CM000669.2:g.83407093T>G GRCh38
NC_000007.13:g.83036409T>G , CM000669.1:g.83036409T>G GRCh37
NC_000007.12:g.82874345T>G NCBI36
NG_021242.1:g.247071A>C
NG_021242.2:g.247071A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.633+4A>C ENSP00000405052.1:n.633+4A>C
ENST00000642232.1:c.813+4A>C ENSP00000494064.1:n.813+4A>C
ENST00000643230.2:c.813+4A>C MANE Select ENSP00000496491.1:n.813+4A>C
ENST00000643441.1:n.798+4A>C
ENST00000307792.7:c.813+4A>C ENSP00000303212.3:n.813+4A>C
ENST00000427262.5:c.633+4A>C ENSP00000405052.1:n.633+4A>C
NM_001178129.1:c.633+4A>C NP_001171600.1:n.633+4A>C
NM_012431.2:c.813+4A>C NP_036563.1:n.813+4A>C
XM_011516715.1:c.813+4A>C XP_011515017.1:n.813+4A>C
NM_012431.3:c.813+4A>C MANE Select NP_036563.1:n.813+4A>C
NM_001178129.2:c.633+4A>C NP_001171600.1:n.633+4A>C