Canonical Allele Identifier: CA2427970815
Gene: SYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47573001_47573003delinsTAG , CM000685.2:g.47573001_47573003delinsTAG GRCh38
NC_000023.10:g.47432400_47432402delinsTAG , CM000685.1:g.47432400_47432402delinsTAG GRCh37
NC_000023.9:g.47317344_47317346delinsTAG NCBI36
NG_008437.1:g.51855_51857delinsCTA
NG_016339.1:g.16885_16887delinsTAG
NG_016339.2:g.16885_16887delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1983-4_1983-2delinsCTA MANE Select ENSP00000295987.7:n.1983-4_1983-2delinsCTA
ENST00000340666.5:c.1983-42_1983-40delinsCTA ENSP00000343206.4:n.1983-42_1983-40delinsCTA
ENST00000640721.1:c.71-42_71-40delinsCTA ENSP00000492857.1:n.71-42_71-40delinsCTA
ENST00000295987.11:c.1983-4_1983-2delinsCTA ENSP00000295987.7:n.1983-4_1983-2delinsCTA
ENST00000340666.4:c.1983-42_1983-40delinsCTA ENSP00000343206.4:n.1983-42_1983-40delinsCTA
NM_006950.3:c.1983-4_1983-2delinsCTA MANE Select NP_008881.2:n.1983-4_1983-2delinsCTA
NM_133499.2:c.1983-42_1983-40delinsCTA NP_598006.1:n.1983-42_1983-40delinsCTA