Canonical Allele Identifier: CA2386325202

Gene: SYNJ1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.32657015G= , CM000683.2:g.32657015G=	GRCh38
NC_000021.8:g.34029325G= , CM000683.1:g.34029325G=	GRCh37
NC_000021.7:g.32951196G=	NCBI36
NG_030017.1:g.76027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382499.7:c.2684C=	ENSP00000371939.2:p.Thr895=
ENST00000433931.7:c.2684C=	ENSP00000409667.2:p.Thr895=
ENST00000630077.3:c.2552C=	ENSP00000487560.1:p.Thr851=
ENST00000674204.1:c.2567C=	ENSP00000501504.1:p.Thr856=
ENST00000674308.1:c.2567C=	ENSP00000501426.1:p.Thr856=
ENST00000674351.1:c.2567C= MANE Select	ENSP00000501530.1:p.Thr856=
ENST00000357345.7:c.2567C=	ENSP00000349903.3:p.Thr856=
ENST00000382491.7:c.2552C=	ENSP00000371931.4:p.Thr851=
ENST00000382499.6:c.2684C=	ENSP00000371939.2:p.Thr895=
ENST00000433931.6:c.2684C=	ENSP00000409667.2:p.Thr895=
ENST00000464778.1:n.354C=
ENST00000630077.2:c.2552C=	ENSP00000487560.1:p.Thr851=
NM_001160302.1:c.2567C=	NP_001153774.1:p.Thr856=
NM_001160306.1:c.2552C=	NP_001153778.1:p.Thr851=
NM_003895.3:c.2684C=	NP_003886.3:p.Thr895=
NM_203446.2:c.2684C=	NP_982271.2:p.Thr895=
XM_017028494.1:c.2567C=	XP_016883983.1:p.Thr856=
XM_017028495.2:c.2669C=	XP_016883984.1:p.Thr890=
XM_017028496.1:c.2567C=	XP_016883985.1:p.Thr856=
XM_017028497.2:c.2684C=	XP_016883986.1:p.Thr895=
XM_017028498.1:c.2567C=	XP_016883987.1:p.Thr856=
XM_017028499.2:c.2669C=	XP_016883988.1:p.Thr890=
XM_017028500.1:c.2567C=	XP_016883989.1:p.Thr856=
XM_017028501.1:c.2567C=	XP_016883990.1:p.Thr856=
XM_017028502.1:c.2567C=	XP_016883991.1:p.Thr856=
XM_017028503.1:c.2567C=	XP_016883992.1:p.Thr856=
XM_017028504.1:c.2567C=	XP_016883993.1:p.Thr856=
XM_017028505.2:c.2669C=	XP_016883994.1:p.Thr890=
NM_001160306.2:c.2552C=	NP_001153778.1:p.Thr851=
NM_203446.3:c.2567C= MANE Select	NP_982271.3:p.Thr856=