Canonical Allele Identifier: CA1721679500

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407112G= , CM000669.2:g.83407112G=	GRCh38
NC_000007.13:g.83036428G= , CM000669.1:g.83036428G=	GRCh37
NC_000007.12:g.82874364G=	NCBI36
NG_021242.1:g.247052C=
NG_021242.2:g.247052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.618C=	ENSP00000405052.1:p.Val206=
ENST00000642232.1:c.798C=	ENSP00000494064.1:p.Val266=
ENST00000643230.2:c.798C= MANE Select	ENSP00000496491.1:p.Val266=
ENST00000643441.1:n.783C=
ENST00000307792.7:c.798C=	ENSP00000303212.3:p.Val266=
ENST00000427262.5:c.618C=	ENSP00000405052.1:p.Val206=
NM_001178129.1:c.618C=	NP_001171600.1:p.Val206=
NM_012431.2:c.798C=	NP_036563.1:p.Val266=
XM_011516715.1:c.798C=	XP_011515017.1:p.Val266=
NM_012431.3:c.798C= MANE Select	NP_036563.1:p.Val266=
NM_001178129.2:c.618C=	NP_001171600.1:p.Val206=