Canonical Allele Identifier: CA456135678

Gene: SEMA3E

Linked Data

• gnomAD v4: 7-83407118-G-A
• MyVariant Identifiers: chr7:g.83036434G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407118G>A , CM000669.2:g.83407118G>A	GRCh38
NC_000007.13:g.83036434G>A , CM000669.1:g.83036434G>A	GRCh37
NC_000007.12:g.82874370G>A	NCBI36
NG_021242.1:g.247046C>T
NG_021242.2:g.247046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.612C>T	ENSP00000405052.1:p.Thr204=
ENST00000642232.1:c.792C>T	ENSP00000494064.1:p.Thr264=
ENST00000643230.2:c.792C>T MANE Select	ENSP00000496491.1:p.Thr264=
ENST00000643441.1:n.777C>T
ENST00000307792.7:c.792C>T	ENSP00000303212.3:p.Thr264=
ENST00000427262.5:c.612C>T	ENSP00000405052.1:p.Thr204=
NM_001178129.1:c.612C>T	NP_001171600.1:p.Thr204=
NM_012431.2:c.792C>T	NP_036563.1:p.Thr264=
XM_011516715.1:c.792C>T	XP_011515017.1:p.Thr264=
NM_012431.3:c.792C>T MANE Select	NP_036563.1:p.Thr264=
NM_001178129.2:c.612C>T	NP_001171600.1:p.Thr204=