Canonical Allele Identifier: CA1346039313
Gene: SYN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188014_12188017delinsTTTC , CM000665.2:g.12188014_12188017delinsTTTC GRCh38
NC_000003.11:g.12229514_12229517delinsTTTC , CM000665.1:g.12229514_12229517delinsTTTC GRCh37
NC_000003.10:g.12204514_12204517delinsTTTC NCBI36
NG_011728.2:g.188627_188630delinsTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+402_1613+405delinsTTTC MANE Select ENSP00000480050.1:n.1613+402_1613+405deli...
ENST00000439861.5:n.1232+402_1232+405delinsTTTC
ENST00000621198.4:c.1613+402_1613+405delinsTTTC ENSP00000480050.1:n.1613+402_1613+405deli...
NM_133625.4:c.1613+402_1613+405delinsTTTC NP_598328.1:n.1613+402_1613+405delinsTTTC...
XM_006713312.2:c.1130+402_1130+405delinsTTTC XP_006713375.1:n.1130+402_1130+405delinsT...
XM_006713313.2:c.842+402_842+405delinsTTTC XP_006713376.1:n.842+402_842+405delinsTTT...
XM_006713312.4:c.1130+402_1130+405delinsTTTC XP_006713375.1:n.1130+402_1130+405delinsT...
XM_017007087.1:c.941+402_941+405delinsTTTC XP_016862576.1:n.941+402_941+405delinsTTT...
NM_133625.5:c.1613+402_1613+405delinsTTTC NP_598328.1:n.1613+402_1613+405delinsTTTC...
NM_133625.6:c.1613+402_1613+405delinsTTTC MANE Select NP_598328.1:n.1613+402_1613+405delinsTTTC...