Canonical Allele Identifier: CA412820702

Gene: SYN1

Linked Data

• MyVariant Identifiers: chrX:g.47432367G>A (hg19) ; chrX:g.47572968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572968G>A , CM000685.2:g.47572968G>A	GRCh38
NC_000023.10:g.47432367G>A , CM000685.1:g.47432367G>A	GRCh37
NC_000023.9:g.47317311G>A	NCBI36
NG_008437.1:g.51890C>T
NG_016339.1:g.16852G>A
NG_016339.2:g.16852G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.2014C>T MANE Select	ENSP00000295987.7:p.Leu672Phe
ENST00000340666.5:c.1983-7C>T	ENSP00000343206.4:n.1983-7C>T
ENST00000640721.1:c.71-7C>T	ENSP00000492857.1:n.71-7C>T
ENST00000295987.11:c.2014C>T	ENSP00000295987.7:p.Leu672Phe
ENST00000340666.4:c.1983-7C>T	ENSP00000343206.4:n.1983-7C>T
NM_006950.3:c.2014C>T MANE Select	NP_008881.2:p.Leu672Phe
NM_133499.2:c.1983-7C>T	NP_598006.1:n.1983-7C>T