Canonical Allele Identifier: CA2386319904

Gene: SYNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32643336_32643344delinsGGGTGGGGA , CM000683.2:g.32643336_32643344delinsGGGTGGGGA	GRCh38
NC_000021.8:g.34015646_34015654delinsGGGTGGGGA , CM000683.1:g.34015646_34015654delinsGGGTGGGGA	GRCh37
NC_000021.7:g.32937517_32937525delinsGGGTGGGGA	NCBI36
NG_030017.1:g.89698_89706delinsTCCCCACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000382499.7:c.3595+66_3595+74delinsTCCCCACCC	ENSP00000371939.2:n.3595+66_3595+74delinsTCCCCACCC
ENST00000433931.7:c.3595+66_3595+74delinsTCCCCACCC	ENSP00000409667.2:n.3595+66_3595+74delinsTCCCCACCC
ENST00000630077.3:c.3377-1378_3377-1370delinsTCCCCACCC	ENSP00000487560.1:n.3377-1378_3377-1370delinsTCCCCACCC
ENST00000674204.1:c.3478+66_3478+74delinsTCCCCACCC	ENSP00000501504.1:n.3478+66_3478+74delinsTCCCCACCC
ENST00000674308.1:c.3478+66_3478+74delinsTCCCCACCC	ENSP00000501426.1:n.3478+66_3478+74delinsTCCCCACCC
ENST00000674351.1:c.3478+66_3478+74delinsTCCCCACCC MANE Select	ENSP00000501530.1:n.3478+66_3478+74delinsTCCCCACCC
ENST00000357345.7:c.3431-1211_3431-1203delinsTCCCCACCC	ENSP00000349903.3:n.3431-1211_3431-1203delinsTCCCCACCC
ENST00000382491.7:c.3377-1378_3377-1370delinsTCCCCACCC	ENSP00000371931.4:n.3377-1378_3377-1370delinsTCCCCACCC
ENST00000382499.6:c.3595+66_3595+74delinsTCCCCACCC	ENSP00000371939.2:n.3595+66_3595+74delinsTCCCCACCC
ENST00000433931.6:c.3595+66_3595+74delinsTCCCCACCC	ENSP00000409667.2:n.3595+66_3595+74delinsTCCCCACCC
ENST00000438952.5:c.105-1211_105-1203delinsTCCCCACCC
ENST00000630077.2:c.3377-1378_3377-1370delinsTCCCCACCC	ENSP00000487560.1:n.3377-1378_3377-1370delinsTCCCCACCC
NM_001160302.1:c.3431-1211_3431-1203delinsTCCCCACCC	NP_001153774.1:n.3431-1211_3431-1203delinsTCCCCACCC
NM_001160306.1:c.3377-1378_3377-1370delinsTCCCCACCC	NP_001153778.1:n.3377-1378_3377-1370delinsTCCCCACCC
NM_003895.3:c.3595+66_3595+74delinsTCCCCACCC	NP_003886.3:n.3595+66_3595+74delinsTCCCCACCC
NM_203446.2:c.3595+66_3595+74delinsTCCCCACCC	NP_982271.2:n.3595+66_3595+74delinsTCCCCACCC
XM_017028494.1:c.3431-1211_3431-1203delinsTCCCCACCC	XP_016883983.1:n.3431-1211_3431-1203delinsTCCCCACCC
XM_017028495.2:c.3580+66_3580+74delinsTCCCCACCC	XP_016883984.1:n.3580+66_3580+74delinsTCCCCACCC
XM_017028496.1:c.3392-1211_3392-1203delinsTCCCCACCC	XP_016883985.1:n.3392-1211_3392-1203delinsTCCCCACCC
XM_017028497.2:c.3548-1211_3548-1203delinsTCCCCACCC	XP_016883986.1:n.3548-1211_3548-1203delinsTCCCCACCC
XM_017028498.1:c.3392-1378_3392-1370delinsTCCCCACCC	XP_016883987.1:n.3392-1378_3392-1370delinsTCCCCACCC
XM_017028499.2:c.3494-1378_3494-1370delinsTCCCCACCC	XP_016883988.1:n.3494-1378_3494-1370delinsTCCCCACCC
XM_017028500.1:c.3478+66_3478+74delinsTCCCCACCC	XP_016883989.1:n.3478+66_3478+74delinsTCCCCACCC
XM_017028501.1:c.3478+66_3478+74delinsTCCCCACCC	XP_016883990.1:n.3478+66_3478+74delinsTCCCCACCC
XM_017028502.1:c.3431-1211_3431-1203delinsTCCCCACCC	XP_016883991.1:n.3431-1211_3431-1203delinsTCCCCACCC
XM_017028503.1:c.3392-1211_3392-1203delinsTCCCCACCC	XP_016883992.1:n.3392-1211_3392-1203delinsTCCCCACCC
XM_017028504.1:c.3392-1378_3392-1370delinsTCCCCACCC	XP_016883993.1:n.3392-1378_3392-1370delinsTCCCCACCC
XM_017028505.2:c.3494-1378_3494-1370delinsTCCCCACCC	XP_016883994.1:n.3494-1378_3494-1370delinsTCCCCACCC
NM_001160306.2:c.3377-1378_3377-1370delinsTCCCCACCC	NP_001153778.1:n.3377-1378_3377-1370delinsTCCCCACCC
NM_203446.3:c.3478+66_3478+74delinsTCCCCACCC MANE Select	NP_982271.3:n.3478+66_3478+74delinsTCCCCACCC