Canonical Allele Identifier: CA2579596632
Gene: SYN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47573037del , CM000685.2:g.47573037del GRCh38
NC_000023.10:g.47432436del , CM000685.1:g.47432436del GRCh37
NC_000023.9:g.47317380del NCBI36
NG_008437.1:g.51825del
NG_016339.1:g.16921del
NG_016339.2:g.16921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1983-34del MANE Select ENSP00000295987.7:n.1983-34del
ENST00000340666.5:c.1983-72del ENSP00000343206.4:n.1983-72del
ENST00000640721.1:c.71-72del ENSP00000492857.1:n.71-72del
ENST00000295987.11:c.1983-34del ENSP00000295987.7:n.1983-34del
ENST00000340666.4:c.1983-72del ENSP00000343206.4:n.1983-72del
NM_006950.3:c.1983-34del MANE Select NP_008881.2:n.1983-34del
NM_133499.2:c.1983-72del NP_598006.1:n.1983-72del