Canonical Allele Identifier: CA1722482101

Gene: SEMA3D

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85096102_85096106delinsAAGCT , CM000669.2:g.85096102_85096106delinsAAGCT	GRCh38
NC_000007.13:g.84725418_84725422delinsAAGCT , CM000669.1:g.84725418_84725422delinsAAGCT	GRCh37
NC_000007.12:g.84563354_84563358delinsAAGCT	NCBI36
NG_051329.1:g.95750_95754delinsAGCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000284136.11:c.312+1699_312+1703delinsAGCTT MANE Select	ENSP00000284136.6:n.312+1699_312+1703delinsAGCTT
ENST00000284136.10:c.312+1699_312+1703delinsAGCTT	ENSP00000284136.6:n.312+1699_312+1703delinsAGCTT
ENST00000444867.1:c.312+1699_312+1703delinsAGCTT	ENSP00000401366.1:n.312+1699_312+1703delinsAGCTT
NM_152754.2:c.312+1699_312+1703delinsAGCTT	NP_689967.2:n.312+1699_312+1703delinsAGCTT
XM_011515960.1:c.312+1699_312+1703delinsAGCTT	XP_011514262.1:n.312+1699_312+1703delinsAGCTT
XM_011515961.1:c.-271+1699_-271+1703delinsAGCTT	XP_011514263.1:n.-271+1699_-271+1703delinsAGCTT
XM_011515961.2:c.-271+1699_-271+1703delinsAGCTT	XP_011514263.1:n.-271+1699_-271+1703delinsAGCTT
XM_017011873.1:c.312+1699_312+1703delinsAGCTT	XP_016867362.1:n.312+1699_312+1703delinsAGCTT
NM_001384900.1:c.312+1699_312+1703delinsAGCTT MANE Select	NP_001371829.1:n.312+1699_312+1703delinsAGCTT
NM_001384901.1:c.312+1699_312+1703delinsAGCTT	NP_001371830.1:n.312+1699_312+1703delinsAGCTT
NM_001384902.1:c.312+1699_312+1703delinsAGCTT	NP_001371831.1:n.312+1699_312+1703delinsAGCTT
NM_001384903.1:c.312+1699_312+1703delinsAGCTT	NP_001371832.1:n.312+1699_312+1703delinsAGCTT
NM_152754.3:c.312+1699_312+1703delinsAGCTT	NP_689967.2:n.312+1699_312+1703delinsAGCTT