Canonical Allele Identifier: CA2427970787

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572879G= , CM000685.2:g.47572879G=	GRCh38
NC_000023.10:g.47432278G= , CM000685.1:g.47432278G=	GRCh37
NC_000023.9:g.47317222G=	NCBI36
NG_008437.1:g.51979C=
NG_016339.1:g.16763G=
NG_016339.2:g.16763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.2103C= MANE Select	ENSP00000295987.7:p.Ser701=
ENST00000340666.5:c.*55C=	ENSP00000343206.4:n.*55C=
ENST00000640721.1:c.153C=	ENSP00000492857.1:p.Ser51=
ENST00000295987.11:c.2103C=	ENSP00000295987.7:p.Ser701=
ENST00000340666.4:c.*55C=	ENSP00000343206.4:n.*55C=
NM_006950.3:c.2103C= MANE Select	NP_008881.2:p.Ser701=
NM_133499.2:c.*55C=	NP_598006.1:n.*55C=