Canonical Allele Identifier: CA2693585122

Gene: SYN1

Linked Data

• gnomAD v4: X-47574256-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574259del , CM000685.2:g.47574259del	GRCh38
NC_000023.10:g.47433658del , CM000685.1:g.47433658del	GRCh37
NC_000023.9:g.47318602del	NCBI36
NG_008437.1:g.50601del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1727del MANE Select	ENSP00000295987.7:p.Lys576ArgfsTer?
ENST00000340666.5:c.1727del	ENSP00000343206.4:p.Lys576ArgfsTer?
ENST00000640721.1:c.70+431del	ENSP00000492857.1:n.70+431del
ENST00000295987.11:c.1727del	ENSP00000295987.7:p.Lys576ArgfsTer?
ENST00000340666.4:c.1727del	ENSP00000343206.4:p.Lys576ArgfsTer?
NM_006950.3:c.1727del MANE Select	NP_008881.2:p.Lys576ArgfsTer?
NM_133499.2:c.1727del	NP_598006.1:p.Lys576ArgfsTer?