Canonical Allele Identifier: CA2579596685

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574541del , CM000685.2:g.47574541del	GRCh38
NC_000023.10:g.47433940del , CM000685.1:g.47433940del	GRCh37
NC_000023.9:g.47318884del	NCBI36
NG_008437.1:g.50317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1443del MANE Select	ENSP00000295987.7:p.Leu481PhefsTer?
ENST00000340666.5:c.1443del	ENSP00000343206.4:p.Leu481PhefsTer?
ENST00000640721.1:c.70+147del	ENSP00000492857.1:n.70+147del
ENST00000295987.11:c.1443del	ENSP00000295987.7:p.Leu481PhefsTer?
ENST00000340666.4:c.1443del	ENSP00000343206.4:p.Leu481PhefsTer?
NM_006950.3:c.1443del MANE Select	NP_008881.2:p.Leu481PhefsTer?
NM_133499.2:c.1443del	NP_598006.1:p.Leu481PhefsTer?