Canonical Allele Identifier: CA412820811
Gene: SYN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47572992G>T , CM000685.2:g.47572992G>T GRCh38
NC_000023.10:g.47432391G>T , CM000685.1:g.47432391G>T GRCh37
NC_000023.9:g.47317335G>T NCBI36
NG_008437.1:g.51866C>A
NG_016339.1:g.16876G>T
NG_016339.2:g.16876G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1990C>A MANE Select ENSP00000295987.7:p.Gln664Lys
ENST00000340666.5:c.1983-31C>A ENSP00000343206.4:n.1983-31C>A
ENST00000640721.1:c.71-31C>A ENSP00000492857.1:n.71-31C>A
ENST00000295987.11:c.1990C>A ENSP00000295987.7:p.Gln664Lys
ENST00000340666.4:c.1983-31C>A ENSP00000343206.4:n.1983-31C>A
NM_006950.3:c.1990C>A MANE Select NP_008881.2:p.Gln664Lys
NM_133499.2:c.1983-31C>A NP_598006.1:n.1983-31C>A