Canonical Allele Identifier: CA1103978929

Gene: SEMA3D

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85122635T>A , CM000669.2:g.85122635T>A	GRCh38
NC_000007.13:g.84751951T>A , CM000669.1:g.84751951T>A	GRCh37
NC_000007.12:g.84589887T>A	NCBI36
NG_051329.1:g.69221A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284136.11:c.-40-704A>T MANE Select	ENSP00000284136.6:n.-40-704A>T
ENST00000444867.1:c.-40-704A>T	ENSP00000401366.1:n.-40-704A>T
XM_011515960.1:c.-40-704A>T	XP_011514262.1:n.-40-704A>T
XM_017011873.1:c.-40-704A>T	XP_016867362.1:n.-40-704A>T
NM_001384900.1:c.-40-704A>T MANE Select	NP_001371829.1:n.-40-704A>T
NM_001384901.1:c.-40-704A>T	NP_001371830.1:n.-40-704A>T
NM_001384902.1:c.-40-704A>T	NP_001371831.1:n.-40-704A>T
NM_001384903.1:c.-40-704A>T	NP_001371832.1:n.-40-704A>T
NM_152754.3:c.-40-704A>T	NP_689967.2:n.-40-704A>T