Canonical Allele Identifier: CA1722482114

Gene: SEMA3D

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85096117_85096118delinsTC , CM000669.2:g.85096117_85096118delinsTC	GRCh38
NC_000007.13:g.84725433_84725434delinsTC , CM000669.1:g.84725433_84725434delinsTC	GRCh37
NC_000007.12:g.84563369_84563370delinsTC	NCBI36
NG_051329.1:g.95738_95739delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284136.11:c.312+1687_312+1688delinsGA MANE Select	ENSP00000284136.6:n.312+1687_312+1688delinsGA
ENST00000284136.10:c.312+1687_312+1688delinsGA	ENSP00000284136.6:n.312+1687_312+1688delinsGA
ENST00000444867.1:c.312+1687_312+1688delinsGA	ENSP00000401366.1:n.312+1687_312+1688delinsGA
NM_152754.2:c.312+1687_312+1688delinsGA	NP_689967.2:n.312+1687_312+1688delinsGA
XM_011515960.1:c.312+1687_312+1688delinsGA	XP_011514262.1:n.312+1687_312+1688delinsGA
XM_011515961.1:c.-271+1687_-271+1688delinsGA	XP_011514263.1:n.-271+1687_-271+1688delinsGA
XM_011515961.2:c.-271+1687_-271+1688delinsGA	XP_011514263.1:n.-271+1687_-271+1688delinsGA
XM_017011873.1:c.312+1687_312+1688delinsGA	XP_016867362.1:n.312+1687_312+1688delinsGA
NM_001384900.1:c.312+1687_312+1688delinsGA MANE Select	NP_001371829.1:n.312+1687_312+1688delinsGA
NM_001384901.1:c.312+1687_312+1688delinsGA	NP_001371830.1:n.312+1687_312+1688delinsGA
NM_001384902.1:c.312+1687_312+1688delinsGA	NP_001371831.1:n.312+1687_312+1688delinsGA
NM_001384903.1:c.312+1687_312+1688delinsGA	NP_001371832.1:n.312+1687_312+1688delinsGA
NM_152754.3:c.312+1687_312+1688delinsGA	NP_689967.2:n.312+1687_312+1688delinsGA