Canonical Allele Identifier: CA2402223880

Gene: SYN3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.33006797G= , CM000684.2:g.33006797G=	GRCh38
NC_000022.10:g.33402782G= , CM000684.1:g.33402782G=	GRCh37
NC_000022.9:g.31732782G=	NCBI36
NG_029545.1:g.56596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358763.7:c.-135C= MANE Select	ENSP00000351614.2:n.-135C=
ENST00000358763.6:c.-135C=	ENSP00000351614.2:n.-135C=
ENST00000412575.1:c.-135C=	ENSP00000388582.1:n.-135C=
ENST00000441821.5:c.-135C=	ENSP00000395794.1:n.-135C=
NM_001135774.1:c.-135C=	NP_001129246.1:n.-135C=
NM_003490.3:c.-135C=	NP_003481.3:n.-135C=
NM_133633.2:c.-135C=	NP_598344.2:n.-135C=
XM_011530405.1:c.-135C=	XP_011528707.1:n.-135C=
XM_011530406.1:c.-135C=	XP_011528708.1:n.-135C=
XM_011530407.1:c.-135C=	XP_011528709.1:n.-135C=
XM_011530408.1:c.-135C=	XP_011528710.1:n.-135C=
XM_011530409.1:c.-135C=	XP_011528711.1:n.-135C=
XM_011530411.1:c.-135C=	XP_011528713.1:n.-135C=
XM_011530413.1:c.-135C=	XP_011528715.1:n.-135C=
XM_011530414.1:c.-135C=	XP_011528716.1:n.-135C=
XR_937927.1:n.350C=
XM_011530405.3:c.-135C=	XP_011528707.1:n.-135C=
XM_011530406.3:c.-135C=	XP_011528708.1:n.-135C=
XM_011530407.3:c.-135C=	XP_011528709.1:n.-135C=
XM_011530408.2:c.-135C=	XP_011528710.1:n.-135C=
XM_017028961.2:c.-135C=	XP_016884450.1:n.-135C=
XM_017028962.2:c.-135C=	XP_016884451.1:n.-135C=
XM_017028963.2:c.-135C=	XP_016884452.1:n.-135C=
XM_017028964.2:c.-135C=	XP_016884453.1:n.-135C=
XR_001755317.2:n.103C=
NM_001135774.2:c.-135C=	NP_001129246.1:n.-135C=
NM_001369907.1:c.-135C=	NP_001356836.1:n.-135C=
NM_001369908.1:c.-135C=	NP_001356837.1:n.-135C=
NM_001369909.1:c.-135C=	NP_001356838.1:n.-135C=
NM_001369910.1:c.-135C=	NP_001356839.1:n.-135C=
NM_003490.4:c.-135C= MANE Select	NP_003481.3:n.-135C=
NM_133633.3:c.-135C=	NP_598344.2:n.-135C=