Canonical Allele Identifier: CA2427971141

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573987_47573988delinsTA , CM000685.2:g.47573987_47573988delinsTA	GRCh38
NC_000023.10:g.47433386_47433387delinsTA , CM000685.1:g.47433386_47433387delinsTA	GRCh37
NC_000023.9:g.47318330_47318331delinsTA	NCBI36
NG_008437.1:g.50870_50871delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1982+14_1982+15delinsTA MANE Select	ENSP00000295987.7:n.1982+14_1982+15delinsTA
ENST00000340666.5:c.1982+14_1982+15delinsTA	ENSP00000343206.4:n.1982+14_1982+15delinsTA
ENST00000640721.1:c.70+700_70+701delinsTA	ENSP00000492857.1:n.70+700_70+701delinsTA
ENST00000295987.11:c.1982+14_1982+15delinsTA	ENSP00000295987.7:n.1982+14_1982+15delinsTA
ENST00000340666.4:c.1982+14_1982+15delinsTA	ENSP00000343206.4:n.1982+14_1982+15delinsTA
NM_006950.3:c.1982+14_1982+15delinsTA MANE Select	NP_008881.2:n.1982+14_1982+15delinsTA
NM_133499.2:c.1982+14_1982+15delinsTA	NP_598006.1:n.1982+14_1982+15delinsTA