Canonical Allele Identifier: CA319437559

Gene: SYNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32727988_32727999del , CM000683.2:g.32727988_32727999del	GRCh38
NC_000021.8:g.34100299_34100310del , CM000683.1:g.34100299_34100310del	GRCh37
NC_000021.7:g.33022170_33022181del	NCBI36
NG_030017.1:g.5051_5062del

Transcript Alleles

HGVS	Amino-acid Change
NM_203446.3:c.-67_-56del MANE Select	NP_982271.3:n.-67_-56del
ENST00000674351.1:c.-67_-56del MANE Select	ENSP00000501530.1:n.-67_-56del
NM_003895.3:c.51_62del	NP_003886.3:p.Gly18_Cys21del
NM_203446.2:c.51_62del	NP_982271.2:p.Gly18_Cys21del
ENST00000382491.7:c.-67_-56del	ENSP00000371931.4:n.-67_-56del
ENST00000382499.6:c.51_62del	ENSP00000371939.2:p.Gly18_Cys21del
ENST00000382499.7:c.51_62del	ENSP00000371939.2:p.Gly18_Cys21del
ENST00000433931.6:c.51_62del	ENSP00000409667.2:p.Gly18_Cys21del
ENST00000433931.7:c.51_62del	ENSP00000409667.2:p.Gly18_Cys21del
ENST00000674308.1:c.-67_-56del	ENSP00000501426.1:n.-67_-56del
XM_017028495.2:c.51_62del	XP_016883984.1:p.Gly18_Cys21del
XM_017028497.2:c.51_62del	XP_016883986.1:p.Gly18_Cys21del
XM_017028499.2:c.51_62del	XP_016883988.1:p.Gly18_Cys21del
XM_017028505.2:c.51_62del	XP_016883994.1:p.Gly18_Cys21del