Canonical Allele Identifier: CA2693585345

Gene: SYN1

Linked Data

• gnomAD v4: X-47574805-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574810del , CM000685.2:g.47574810del	GRCh38
NC_000023.10:g.47434209del , CM000685.1:g.47434209del	GRCh37
NC_000023.9:g.47319153del	NCBI36
NG_008437.1:g.50052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1306-31del MANE Select	ENSP00000295987.7:n.1306-31del
ENST00000340666.5:c.1306-31del	ENSP00000343206.4:n.1306-31del
ENST00000295987.11:c.1306-31del	ENSP00000295987.7:n.1306-31del
ENST00000340666.4:c.1306-31del	ENSP00000343206.4:n.1306-31del
NM_006950.3:c.1306-31del MANE Select	NP_008881.2:n.1306-31del
NM_133499.2:c.1306-31del	NP_598006.1:n.1306-31del