Canonical Allele Identifier: CA367923272

Gene: SEMA3E

Linked Data

• COSMIC: COSM6344992
• MyVariant Identifiers: chr7:g.83021943G>T (hg19) ; chr7:g.83392627G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392627G>T , CM000669.2:g.83392627G>T	GRCh38
NC_000007.13:g.83021943G>T , CM000669.1:g.83021943G>T	GRCh37
NC_000007.12:g.82859879G>T	NCBI36
NG_021242.1:g.261537C>A
NG_021242.2:g.261537C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.1415C>A	ENSP00000405052.1:p.Ala472Asp
ENST00000642232.1:c.1595C>A	ENSP00000494064.1:p.Ala532Asp
ENST00000643230.2:c.1595C>A MANE Select	ENSP00000496491.1:p.Ala532Asp
ENST00000643441.1:n.1580C>A
ENST00000307792.7:c.1595C>A	ENSP00000303212.3:p.Ala532Asp
ENST00000427262.5:c.1415C>A	ENSP00000405052.1:p.Ala472Asp
NM_001178129.1:c.1415C>A	NP_001171600.1:p.Ala472Asp
NM_012431.2:c.1595C>A	NP_036563.1:p.Ala532Asp
XM_011516715.1:c.1595C>A	XP_011515017.1:p.Ala532Asp
NM_012431.3:c.1595C>A MANE Select	NP_036563.1:p.Ala532Asp
NM_001178129.2:c.1415C>A	NP_001171600.1:p.Ala472Asp