Canonical Allele Identifier: CA456133445
Gene: SEMA3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.83021903G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392587G>A , CM000669.2:g.83392587G>A GRCh38
NC_000007.13:g.83021903G>A , CM000669.1:g.83021903G>A GRCh37
NC_000007.12:g.82859839G>A NCBI36
NG_021242.1:g.261577C>T
NG_021242.2:g.261577C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1455C>T ENSP00000405052.1:p.Ser485=
ENST00000642232.1:c.1635C>T ENSP00000494064.1:p.Ser545=
ENST00000643230.2:c.1635C>T MANE Select ENSP00000496491.1:p.Ser545=
ENST00000643441.1:n.1620C>T
ENST00000307792.7:c.1635C>T ENSP00000303212.3:p.Ser545=
ENST00000427262.5:c.1455C>T ENSP00000405052.1:p.Ser485=
NM_001178129.1:c.1455C>T NP_001171600.1:p.Ser485=
NM_012431.2:c.1635C>T NP_036563.1:p.Ser545=
XM_011516715.1:c.1635C>T XP_011515017.1:p.Ser545=
NM_012431.3:c.1635C>T MANE Select NP_036563.1:p.Ser545=
NM_001178129.2:c.1455C>T NP_001171600.1:p.Ser485=