Canonical Allele Identifier: CA1346039314
Gene: SYN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188015_12188017delinsTTC , CM000665.2:g.12188015_12188017delinsTTC GRCh38
NC_000003.11:g.12229515_12229517delinsTTC , CM000665.1:g.12229515_12229517delinsTTC GRCh37
NC_000003.10:g.12204515_12204517delinsTTC NCBI36
NG_011728.2:g.188628_188630delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+403_1613+405delinsTTC MANE Select ENSP00000480050.1:n.1613+403_1613+405deli...
ENST00000439861.5:n.1232+403_1232+405delinsTTC
ENST00000621198.4:c.1613+403_1613+405delinsTTC ENSP00000480050.1:n.1613+403_1613+405deli...
NM_133625.4:c.1613+403_1613+405delinsTTC NP_598328.1:n.1613+403_1613+405delinsTTC
XM_006713312.2:c.1130+403_1130+405delinsTTC XP_006713375.1:n.1130+403_1130+405delinsT...
XM_006713313.2:c.842+403_842+405delinsTTC XP_006713376.1:n.842+403_842+405delinsTTC...
XM_006713312.4:c.1130+403_1130+405delinsTTC XP_006713375.1:n.1130+403_1130+405delinsT...
XM_017007087.1:c.941+403_941+405delinsTTC XP_016862576.1:n.941+403_941+405delinsTTC...
NM_133625.5:c.1613+403_1613+405delinsTTC NP_598328.1:n.1613+403_1613+405delinsTTC
NM_133625.6:c.1613+403_1613+405delinsTTC MANE Select NP_598328.1:n.1613+403_1613+405delinsTTC