Canonical Allele Identifier: CA161171033

Gene: SEMA3E

Linked Data

• dbSNP Id: rs545427928
• gnomAD v2: 7-83036294-A-G
• gnomAD v3: 7-83406978-A-G
• gnomAD v4: 7-83406978-A-G
• MyVariant Identifiers: chr7:g.83036294A>G (hg19) ; chr7:g.83406978A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83406978A>G , CM000669.2:g.83406978A>G	GRCh38
NC_000007.13:g.83036294A>G , CM000669.1:g.83036294A>G	GRCh37
NC_000007.12:g.82874230A>G	NCBI36
NG_021242.1:g.247186T>C
NG_021242.2:g.247186T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.633+119T>C	ENSP00000405052.1:n.633+119T>C
ENST00000642232.1:c.813+119T>C	ENSP00000494064.1:n.813+119T>C
ENST00000643230.2:c.813+119T>C MANE Select	ENSP00000496491.1:n.813+119T>C
ENST00000643441.1:n.798+119T>C
ENST00000307792.7:c.813+119T>C	ENSP00000303212.3:n.813+119T>C
ENST00000427262.5:c.633+119T>C	ENSP00000405052.1:n.633+119T>C
NM_001178129.1:c.633+119T>C	NP_001171600.1:n.633+119T>C
NM_012431.2:c.813+119T>C	NP_036563.1:n.813+119T>C
XM_011516715.1:c.813+119T>C	XP_011515017.1:n.813+119T>C
NM_012431.3:c.813+119T>C MANE Select	NP_036563.1:n.813+119T>C
NM_001178129.2:c.633+119T>C	NP_001171600.1:n.633+119T>C