Canonical Allele Identifier: CA456135711

Gene: SEMA3E

Linked Data

• MyVariant Identifiers: chr7:g.83036443T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407127T>C , CM000669.2:g.83407127T>C	GRCh38
NC_000007.13:g.83036443T>C , CM000669.1:g.83036443T>C	GRCh37
NC_000007.12:g.82874379T>C	NCBI36
NG_021242.1:g.247037A>G
NG_021242.2:g.247037A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.603A>G	ENSP00000405052.1:p.Ala201=
ENST00000642232.1:c.783A>G	ENSP00000494064.1:p.Ala261=
ENST00000643230.2:c.783A>G MANE Select	ENSP00000496491.1:p.Ala261=
ENST00000643441.1:n.768A>G
ENST00000307792.7:c.783A>G	ENSP00000303212.3:p.Ala261=
ENST00000427262.5:c.603A>G	ENSP00000405052.1:p.Ala201=
NM_001178129.1:c.603A>G	NP_001171600.1:p.Ala201=
NM_012431.2:c.783A>G	NP_036563.1:p.Ala261=
XM_011516715.1:c.783A>G	XP_011515017.1:p.Ala261=
NM_012431.3:c.783A>G MANE Select	NP_036563.1:p.Ala261=
NM_001178129.2:c.603A>G	NP_001171600.1:p.Ala201=