Canonical Allele Identifier: CA2693585260

Gene: SYN1

Linked Data

• gnomAD v4: X-47574611-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574614_47574615del , CM000685.2:g.47574614_47574615del	GRCh38
NC_000023.10:g.47434013_47434014del , CM000685.1:g.47434013_47434014del	GRCh37
NC_000023.9:g.47318957_47318958del	NCBI36
NG_008437.1:g.50245_50246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1394-23_1394-22del MANE Select	ENSP00000295987.7:n.1394-23_1394-22del
ENST00000340666.5:c.1394-23_1394-22del	ENSP00000343206.4:n.1394-23_1394-22del
ENST00000640721.1:c.70+75_70+76del	ENSP00000492857.1:n.70+75_70+76del
ENST00000295987.11:c.1394-23_1394-22del	ENSP00000295987.7:n.1394-23_1394-22del
ENST00000340666.4:c.1394-23_1394-22del	ENSP00000343206.4:n.1394-23_1394-22del
NM_006950.3:c.1394-23_1394-22del MANE Select	NP_008881.2:n.1394-23_1394-22del
NM_133499.2:c.1394-23_1394-22del	NP_598006.1:n.1394-23_1394-22del