Canonical Allele Identifier: CA2521737594
Gene: SYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574229_47574241del , CM000685.2:g.47574229_47574241del GRCh38
NC_000023.10:g.47433628_47433640del , CM000685.1:g.47433628_47433640del GRCh37
NC_000023.9:g.47318572_47318584del NCBI36
NG_008437.1:g.50617_50629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1743_1755del MANE Select ENSP00000295987.7:p.Pro582SerfsTer?
ENST00000340666.5:c.1743_1755del ENSP00000343206.4:p.Pro582SerfsTer?
ENST00000640721.1:c.70+447_70+459del ENSP00000492857.1:n.70+447_70+459del
ENST00000295987.11:c.1743_1755del ENSP00000295987.7:p.Pro582SerfsTer?
ENST00000340666.4:c.1743_1755del ENSP00000343206.4:p.Pro582SerfsTer?
NM_006950.3:c.1743_1755del MANE Select NP_008881.2:p.Pro582SerfsTer?
NM_133499.2:c.1743_1755del NP_598006.1:p.Pro582SerfsTer?