Canonical Allele Identifier: CA367923235

Gene: SEMA3E

Linked Data

• dbSNP Id: rs1376614893
• gnomAD v2: 7-83021935-G-C
• gnomAD v4: 7-83392619-G-C
• MyVariant Identifiers: chr7:g.83021935G>C (hg19) ; chr7:g.83392619G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392619G>C , CM000669.2:g.83392619G>C	GRCh38
NC_000007.13:g.83021935G>C , CM000669.1:g.83021935G>C	GRCh37
NC_000007.12:g.82859871G>C	NCBI36
NG_021242.1:g.261545C>G
NG_021242.2:g.261545C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.1423C>G	ENSP00000405052.1:p.Pro475Ala
ENST00000642232.1:c.1603C>G	ENSP00000494064.1:p.Pro535Ala
ENST00000643230.2:c.1603C>G MANE Select	ENSP00000496491.1:p.Pro535Ala
ENST00000643441.1:n.1588C>G
ENST00000307792.7:c.1603C>G	ENSP00000303212.3:p.Pro535Ala
ENST00000427262.5:c.1423C>G	ENSP00000405052.1:p.Pro475Ala
NM_001178129.1:c.1423C>G	NP_001171600.1:p.Pro475Ala
NM_012431.2:c.1603C>G	NP_036563.1:p.Pro535Ala
XM_011516715.1:c.1603C>G	XP_011515017.1:p.Pro535Ala
NM_012431.3:c.1603C>G MANE Select	NP_036563.1:p.Pro535Ala
NM_001178129.2:c.1423C>G	NP_001171600.1:p.Pro475Ala