Canonical Allele Identifier: CA1721679519

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407163A= , CM000669.2:g.83407163A=	GRCh38
NC_000007.13:g.83036479A= , CM000669.1:g.83036479A=	GRCh37
NC_000007.12:g.82874415A=	NCBI36
NG_021242.1:g.247001T=
NG_021242.2:g.247001T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.567T=	ENSP00000405052.1:p.Thr189=
ENST00000642232.1:c.747T=	ENSP00000494064.1:p.Thr249=
ENST00000643230.2:c.747T= MANE Select	ENSP00000496491.1:p.Thr249=
ENST00000643441.1:n.732T=
ENST00000644381.1:n.310T=
ENST00000307792.7:c.747T=	ENSP00000303212.3:p.Thr249=
ENST00000427262.5:c.567T=	ENSP00000405052.1:p.Thr189=
NM_001178129.1:c.567T=	NP_001171600.1:p.Thr189=
NM_012431.2:c.747T=	NP_036563.1:p.Thr249=
XM_011516715.1:c.747T=	XP_011515017.1:p.Thr249=
NM_012431.3:c.747T= MANE Select	NP_036563.1:p.Thr249=
NM_001178129.2:c.567T=	NP_001171600.1:p.Thr189=