Canonical Allele Identifier: CA2656325001

Gene: SYN3

Linked Data

• gnomAD v4: 22-33006869-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.33006869C>G , CM000684.2:g.33006869C>G	GRCh38
NC_000022.10:g.33402854C>G , CM000684.1:g.33402854C>G	GRCh37
NC_000022.9:g.31732854C>G	NCBI36
NG_029545.1:g.56524G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358763.7:c.-162-45G>C MANE Select	ENSP00000351614.2:n.-162-45G>C
ENST00000358763.6:c.-162-45G>C	ENSP00000351614.2:n.-162-45G>C
ENST00000412575.1:c.-162-45G>C	ENSP00000388582.1:n.-162-45G>C
ENST00000441821.5:c.-162-45G>C	ENSP00000395794.1:n.-162-45G>C
NM_001135774.1:c.-162-45G>C	NP_001129246.1:n.-162-45G>C
XM_011530405.1:c.-162-45G>C	XP_011528707.1:n.-162-45G>C
XM_011530406.1:c.-162-45G>C	XP_011528708.1:n.-162-45G>C
XM_011530407.1:c.-162-45G>C	XP_011528709.1:n.-162-45G>C
XM_011530408.1:c.-159-48G>C	XP_011528710.1:n.-159-48G>C
XM_011530409.1:c.-162-45G>C	XP_011528711.1:n.-162-45G>C
XM_011530411.1:c.-162-45G>C	XP_011528713.1:n.-162-45G>C
XM_011530413.1:c.-162-45G>C	XP_011528715.1:n.-162-45G>C
XM_011530414.1:c.-162-45G>C	XP_011528716.1:n.-162-45G>C
XR_937927.1:n.323-45G>C
XM_011530405.3:c.-162-45G>C	XP_011528707.1:n.-162-45G>C
XM_011530406.3:c.-162-45G>C	XP_011528708.1:n.-162-45G>C
XM_011530407.3:c.-162-45G>C	XP_011528709.1:n.-162-45G>C
XM_011530408.2:c.-159-48G>C	XP_011528710.1:n.-159-48G>C
XM_017028961.2:c.-162-45G>C	XP_016884450.1:n.-162-45G>C
XM_017028962.2:c.-162-45G>C	XP_016884451.1:n.-162-45G>C
XM_017028963.2:c.-159-48G>C	XP_016884452.1:n.-159-48G>C
XM_017028964.2:c.-159-48G>C	XP_016884453.1:n.-159-48G>C
XR_001755317.2:n.76-45G>C
NM_001135774.2:c.-162-45G>C	NP_001129246.1:n.-162-45G>C
NM_001369907.1:c.-159-48G>C	NP_001356836.1:n.-159-48G>C
NM_001369908.1:c.-162-45G>C	NP_001356837.1:n.-162-45G>C
NM_001369909.1:c.-159-48G>C	NP_001356838.1:n.-159-48G>C
NM_001369910.1:c.-159-48G>C	NP_001356839.1:n.-159-48G>C
NM_003490.4:c.-162-45G>C MANE Select	NP_003481.3:n.-162-45G>C