Canonical Allele Identifier: CA2427971346

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574600_47574604delinsAGAGG , CM000685.2:g.47574600_47574604delinsAGAGG	GRCh38
NC_000023.10:g.47433999_47434003delinsAGAGG , CM000685.1:g.47433999_47434003delinsAGAGG	GRCh37
NC_000023.9:g.47318943_47318947delinsAGAGG	NCBI36
NG_008437.1:g.50254_50258delinsCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1394-14_1394-10delinsCCTCT MANE Select	ENSP00000295987.7:n.1394-14_1394-10delinsCCTCT
ENST00000340666.5:c.1394-14_1394-10delinsCCTCT	ENSP00000343206.4:n.1394-14_1394-10delinsCCTCT
ENST00000640721.1:c.70+84_70+88delinsCCTCT	ENSP00000492857.1:n.70+84_70+88delinsCCTCT
ENST00000295987.11:c.1394-14_1394-10delinsCCTCT	ENSP00000295987.7:n.1394-14_1394-10delinsCCTCT
ENST00000340666.4:c.1394-14_1394-10delinsCCTCT	ENSP00000343206.4:n.1394-14_1394-10delinsCCTCT
NM_006950.3:c.1394-14_1394-10delinsCCTCT MANE Select	NP_008881.2:n.1394-14_1394-10delinsCCTCT
NM_133499.2:c.1394-14_1394-10delinsCCTCT	NP_598006.1:n.1394-14_1394-10delinsCCTCT