Canonical Allele Identifier: CA367930372

Gene: SEMA3E

Linked Data

• gnomAD v4: 7-83407198-C-A
• MyVariant Identifiers: chr7:g.83036514C>A (hg19) ; chr7:g.83407198C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407198C>A , CM000669.2:g.83407198C>A	GRCh38
NC_000007.13:g.83036514C>A , CM000669.1:g.83036514C>A	GRCh37
NC_000007.12:g.82874450C>A	NCBI36
NG_021242.1:g.246966G>T
NG_021242.2:g.246966G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000427262.6:c.532G>T	ENSP00000405052.1:p.Asp178Tyr
ENST00000642232.1:c.712G>T	ENSP00000494064.1:p.Asp238Tyr
ENST00000643230.2:c.712G>T MANE Select	ENSP00000496491.1:p.Asp238Tyr
ENST00000643441.1:n.697G>T
ENST00000644381.1:n.275G>T
ENST00000307792.7:c.712G>T	ENSP00000303212.3:p.Asp238Tyr
ENST00000427262.5:c.532G>T	ENSP00000405052.1:p.Asp178Tyr
NM_001178129.1:c.532G>T	NP_001171600.1:p.Asp178Tyr
NM_012431.2:c.712G>T	NP_036563.1:p.Asp238Tyr
XM_011516715.1:c.712G>T	XP_011515017.1:p.Asp238Tyr
NM_012431.3:c.712G>T MANE Select	NP_036563.1:p.Asp238Tyr
NM_001178129.2:c.532G>T	NP_001171600.1:p.Asp178Tyr