Canonical Allele Identifier: CA2427976079

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47588427_47588428delinsTC , CM000685.2:g.47588427_47588428delinsTC	GRCh38
NC_000023.10:g.47447826_47447827delinsTC , CM000685.1:g.47447826_47447827delinsTC	GRCh37
NC_000023.9:g.47332770_47332771delinsTC	NCBI36
NG_008437.1:g.36430_36431delinsGA
NG_012533.1:g.11137_11138delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.775-10927_775-10926delinsGA MANE Select	ENSP00000295987.7:n.775-10927_775-10926delinsGA
ENST00000340666.5:c.775-10927_775-10926delinsGA	ENSP00000343206.4:n.775-10927_775-10926delinsGA
ENST00000295987.11:c.775-10927_775-10926delinsGA	ENSP00000295987.7:n.775-10927_775-10926delinsGA
ENST00000340666.4:c.775-10927_775-10926delinsGA	ENSP00000343206.4:n.775-10927_775-10926delinsGA
NM_006950.3:c.775-10927_775-10926delinsGA MANE Select	NP_008881.2:n.775-10927_775-10926delinsGA
NM_133499.2:c.775-10927_775-10926delinsGA	NP_598006.1:n.775-10927_775-10926delinsGA