Canonical Allele Identifier: CA1722476872

Gene: SEMA3D

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85084431A= , CM000669.2:g.85084431A=	GRCh38
NC_000007.13:g.84713747A= , CM000669.1:g.84713747A=	GRCh37
NC_000007.12:g.84551683A=	NCBI36
NG_051329.1:g.107425T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000284136.11:c.313-2852T= MANE Select	ENSP00000284136.6:n.313-2852T=
ENST00000284136.10:c.313-2852T=	ENSP00000284136.6:n.313-2852T=
ENST00000444867.1:c.313-2852T=	ENSP00000401366.1:n.313-2852T=
NM_152754.2:c.313-2852T=	NP_689967.2:n.313-2852T=
XM_011515960.1:c.313-2852T=	XP_011514262.1:n.313-2852T=
XM_011515961.1:c.-270-2852T=	XP_011514263.1:n.-270-2852T=
XM_011515961.2:c.-270-2852T=	XP_011514263.1:n.-270-2852T=
XM_017011873.1:c.313-2852T=	XP_016867362.1:n.313-2852T=
NM_001384900.1:c.313-2852T= MANE Select	NP_001371829.1:n.313-2852T=
NM_001384901.1:c.313-2852T=	NP_001371830.1:n.313-2852T=
NM_001384902.1:c.313-2852T=	NP_001371831.1:n.313-2852T=
NM_001384903.1:c.313-2852T=	NP_001371832.1:n.313-2852T=
NM_152754.3:c.313-2852T=	NP_689967.2:n.313-2852T=