Canonical Allele Identifier: CA875829591

Gene: SYN1

Linked Data

• dbSNP Id: rs1490905654
• MyVariant Identifiers: chrX:g.47447925G>C (hg19) ; chrX:g.47588526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47588526G>C , CM000685.2:g.47588526G>C	GRCh38
NC_000023.10:g.47447925G>C , CM000685.1:g.47447925G>C	GRCh37
NC_000023.9:g.47332869G>C	NCBI36
NG_008437.1:g.36332C>G
NG_012533.1:g.11236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.775-11025C>G MANE Select	ENSP00000295987.7:n.775-11025C>G
ENST00000340666.5:c.775-11025C>G	ENSP00000343206.4:n.775-11025C>G
ENST00000295987.11:c.775-11025C>G	ENSP00000295987.7:n.775-11025C>G
ENST00000340666.4:c.775-11025C>G	ENSP00000343206.4:n.775-11025C>G
NM_006950.3:c.775-11025C>G MANE Select	NP_008881.2:n.775-11025C>G
NM_133499.2:c.775-11025C>G	NP_598006.1:n.775-11025C>G