Canonical Allele Identifier: CA1722439212

Gene: SEMA3D

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84999673T= , CM000669.2:g.84999673T=	GRCh38
NC_000007.13:g.84628989T= , CM000669.1:g.84628989T=	GRCh37
NC_000007.12:g.84466925T=	NCBI36
NG_051329.1:g.192183A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284136.11:c.2101A= MANE Select	ENSP00000284136.6:p.Lys701=
ENST00000284136.10:c.2101A=	ENSP00000284136.6:p.Lys701=
ENST00000484038.1:n.1227A=
NM_152754.2:c.2101A=	NP_689967.2:p.Lys701=
XM_011515960.1:c.2101A=	XP_011514262.1:p.Lys701=
XM_011515961.1:c.1519A=	XP_011514263.1:p.Lys507=
XM_011515962.1:c.1018A=	XP_011514264.1:p.Lys340=
XM_011515961.2:c.1519A=	XP_011514263.1:p.Lys507=
XM_017011873.1:c.2101A=	XP_016867362.1:p.Lys701=
NM_001384900.1:c.2101A= MANE Select	NP_001371829.1:p.Lys701=
NM_001384901.1:c.2101A=	NP_001371830.1:p.Lys701=
NM_001384902.1:c.2101A=	NP_001371831.1:p.Lys701=
NM_001384903.1:c.2101A=	NP_001371832.1:p.Lys701=
NM_152754.3:c.2101A=	NP_689967.2:p.Lys701=