Canonical Allele Identifier: CA2683556127

Gene: SEMA3E

Linked Data

• gnomAD v4: 7-83392517-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83392519del , CM000669.2:g.83392519del	GRCh38
NC_000007.13:g.83021835del , CM000669.1:g.83021835del	GRCh37
NC_000007.12:g.82859771del	NCBI36
NG_021242.1:g.261646del
NG_021242.2:g.261646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.1487+37del	ENSP00000405052.1:n.1487+37del
ENST00000642232.1:c.1667+37del	ENSP00000494064.1:n.1667+37del
ENST00000643230.2:c.1667+37del MANE Select	ENSP00000496491.1:n.1667+37del
ENST00000643441.1:n.1652+37del
ENST00000307792.7:c.1667+37del	ENSP00000303212.3:n.1667+37del
ENST00000427262.5:c.1487+37del	ENSP00000405052.1:n.1487+37del
NM_001178129.1:c.1487+37del	NP_001171600.1:n.1487+37del
NM_012431.2:c.1667+37del	NP_036563.1:n.1667+37del
XM_011516715.1:c.1667+37del	XP_011515017.1:n.1667+37del
NM_012431.3:c.1667+37del MANE Select	NP_036563.1:n.1667+37del
NM_001178129.2:c.1487+37del	NP_001171600.1:n.1487+37del