Canonical Allele Identifier: CA641483655

Gene: SYN1

Linked Data

• dbSNP Id: rs996728462
• gnomAD v2: X-47432656-G-T
• gnomAD v3: X-47573257-G-T
• gnomAD v4: X-47573257-G-T
• MyVariant Identifiers: chrX:g.47432656G>T (hg19) ; chrX:g.47573257G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573257G>T , CM000685.2:g.47573257G>T	GRCh38
NC_000023.10:g.47432656G>T , CM000685.1:g.47432656G>T	GRCh37
NC_000023.9:g.47317600G>T	NCBI36
NG_008437.1:g.51601C>A
NG_016339.1:g.17141G>T
NG_016339.2:g.17141G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-258C>A MANE Select	ENSP00000295987.7:n.1983-258C>A
ENST00000340666.5:c.1983-296C>A	ENSP00000343206.4:n.1983-296C>A
ENST00000640721.1:c.71-296C>A	ENSP00000492857.1:n.71-296C>A
ENST00000295987.11:c.1983-258C>A	ENSP00000295987.7:n.1983-258C>A
ENST00000340666.4:c.1983-296C>A	ENSP00000343206.4:n.1983-296C>A
NM_006950.3:c.1983-258C>A MANE Select	NP_008881.2:n.1983-258C>A
NM_133499.2:c.1983-296C>A	NP_598006.1:n.1983-296C>A