Canonical Allele Identifier: CA14938470

Gene: SYN3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32512751T>C , CM000684.2:g.32512751T>C	GRCh38
NC_000022.10:g.32908738T>C , CM000684.1:g.32908738T>C	GRCh37
NC_000022.9:g.31238738T>C	NCBI36
NG_029545.1:g.550640A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358763.7:c.*941A>G MANE Select	ENSP00000351614.2:n.*941A>G
ENST00000358763.6:c.*941A>G	ENSP00000351614.2:n.*941A>G
NM_001135774.1:c.*941A>G	NP_001129246.1:n.*941A>G
NM_003490.3:c.*941A>G	NP_003481.3:n.*941A>G
NM_133633.2:c.*1057A>G	NP_598344.2:n.*1057A>G
XM_011530405.1:c.*941A>G	XP_011528707.1:n.*941A>G
XM_011530406.1:c.*941A>G	XP_011528708.1:n.*941A>G
XM_011530407.1:c.*941A>G	XP_011528709.1:n.*941A>G
XM_011530408.1:c.*941A>G	XP_011528710.1:n.*941A>G
XM_011530409.1:c.*941A>G	XP_011528711.1:n.*941A>G
XM_011530410.1:c.*941A>G	XP_011528712.1:n.*941A>G
XM_011530412.1:c.*941A>G	XP_011528714.1:n.*941A>G
XR_937927.1:n.3168A>G
XM_011530405.3:c.*941A>G	XP_011528707.1:n.*941A>G
XM_011530406.3:c.*941A>G	XP_011528708.1:n.*941A>G
XM_011530407.3:c.*941A>G	XP_011528709.1:n.*941A>G
XM_011530408.2:c.*941A>G	XP_011528710.1:n.*941A>G
XM_011530410.3:c.*941A>G	XP_011528712.1:n.*941A>G
XM_017028961.2:c.*941A>G	XP_016884450.1:n.*941A>G
XM_017028962.2:c.*941A>G	XP_016884451.1:n.*941A>G
XM_017028963.2:c.*941A>G	XP_016884452.1:n.*941A>G
XM_017028964.2:c.*941A>G	XP_016884453.1:n.*941A>G
XM_017028965.2:c.*941A>G	XP_016884454.1:n.*941A>G
XR_001755317.2:n.2833A>G
NM_001135774.2:c.*941A>G	NP_001129246.1:n.*941A>G
NM_001369907.1:c.*941A>G	NP_001356836.1:n.*941A>G
NM_001369908.1:c.*941A>G	NP_001356837.1:n.*941A>G
NM_001369909.1:c.*941A>G	NP_001356838.1:n.*941A>G
NM_001369910.1:c.*941A>G	NP_001356839.1:n.*941A>G
NM_003490.4:c.*941A>G MANE Select	NP_003481.3:n.*941A>G
NM_133633.3:c.*1057A>G	NP_598344.2:n.*1057A>G