Canonical Allele Identifier: CA2579596639
Gene: SYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47573053_47573054insTGGGGAGGA , CM000685.2:g.47573053_47573054insTGGGGAGGA GRCh38
NC_000023.10:g.47432452_47432453insTGGGGAGGA , CM000685.1:g.47432452_47432453insTGGGGAGGA GRCh37
NC_000023.9:g.47317396_47317397insTGGGGAGGA NCBI36
NG_008437.1:g.51812_51813insATCCTCCCC
NG_016339.1:g.16937_16938insTGGGGAGGA
NG_016339.2:g.16937_16938insTGGGGAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1983-47_1983-46insATCCTCCCC MANE Select ENSP00000295987.7:n.1983-47_1983-46insATCCTCCCC
ENST00000340666.5:c.1983-85_1983-84insATCCTCCCC ENSP00000343206.4:n.1983-85_1983-84insATCCTCCCC
ENST00000640721.1:c.71-85_71-84insATCCTCCCC ENSP00000492857.1:n.71-85_71-84insATCCTCCCC
ENST00000295987.11:c.1983-47_1983-46insATCCTCCCC ENSP00000295987.7:n.1983-47_1983-46insATCCTCCCC
ENST00000340666.4:c.1983-85_1983-84insATCCTCCCC ENSP00000343206.4:n.1983-85_1983-84insATCCTCCCC
NM_006950.3:c.1983-47_1983-46insATCCTCCCC MANE Select NP_008881.2:n.1983-47_1983-46insATCCTCCCC
NM_133499.2:c.1983-85_1983-84insATCCTCCCC NP_598006.1:n.1983-85_1983-84insATCCTCCCC