Canonical Allele Identifier: CA367930239

Gene: SEMA3E

Linked Data

• MyVariant Identifiers: chr7:g.83036456T>G (hg19) ; chr7:g.83407140T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407140T>G , CM000669.2:g.83407140T>G	GRCh38
NC_000007.13:g.83036456T>G , CM000669.1:g.83036456T>G	GRCh37
NC_000007.12:g.82874392T>G	NCBI36
NG_021242.1:g.247024A>C
NG_021242.2:g.247024A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.590A>C	ENSP00000405052.1:p.Asn197Thr
ENST00000642232.1:c.770A>C	ENSP00000494064.1:p.Asn257Thr
ENST00000643230.2:c.770A>C MANE Select	ENSP00000496491.1:p.Asn257Thr
ENST00000643441.1:n.755A>C
ENST00000644381.1:n.333A>C
ENST00000307792.7:c.770A>C	ENSP00000303212.3:p.Asn257Thr
ENST00000427262.5:c.590A>C	ENSP00000405052.1:p.Asn197Thr
NM_001178129.1:c.590A>C	NP_001171600.1:p.Asn197Thr
NM_012431.2:c.770A>C	NP_036563.1:p.Asn257Thr
XM_011516715.1:c.770A>C	XP_011515017.1:p.Asn257Thr
NM_012431.3:c.770A>C MANE Select	NP_036563.1:p.Asn257Thr
NM_001178129.2:c.590A>C	NP_001171600.1:p.Asn197Thr