Canonical Allele Identifier: CA2427970823

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573026_47573039delinsGGAGGAAGGGGGAA , CM000685.2:g.47573026_47573039delinsGGAGGAAGGGGGAA	GRCh38
NC_000023.10:g.47432425_47432438delinsGGAGGAAGGGGGAA , CM000685.1:g.47432425_47432438delinsGGAGGAAGGGGGAA	GRCh37
NC_000023.9:g.47317369_47317382delinsGGAGGAAGGGGGAA	NCBI36
NG_008437.1:g.51819_51832delinsTTCCCCCTTCCTCC
NG_016339.1:g.16910_16923delinsGGAGGAAGGGGGAA
NG_016339.2:g.16910_16923delinsGGAGGAAGGGGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-40_1983-27delinsTTCCCCCTTCCTCC MANE Select	ENSP00000295987.7:n.1983-40_1983-27delinsTTCCCCCTTCCTCC
ENST00000340666.5:c.1983-78_1983-65delinsTTCCCCCTTCCTCC	ENSP00000343206.4:n.1983-78_1983-65delinsTTCCCCCTTCCTCC
ENST00000640721.1:c.71-78_71-65delinsTTCCCCCTTCCTCC	ENSP00000492857.1:n.71-78_71-65delinsTTCCCCCTTCCTCC
ENST00000295987.11:c.1983-40_1983-27delinsTTCCCCCTTCCTCC	ENSP00000295987.7:n.1983-40_1983-27delinsTTCCCCCTTCCTCC
ENST00000340666.4:c.1983-78_1983-65delinsTTCCCCCTTCCTCC	ENSP00000343206.4:n.1983-78_1983-65delinsTTCCCCCTTCCTCC
NM_006950.3:c.1983-40_1983-27delinsTTCCCCCTTCCTCC MANE Select	NP_008881.2:n.1983-40_1983-27delinsTTCCCCCTTCCTCC
NM_133499.2:c.1983-78_1983-65delinsTTCCCCCTTCCTCC	NP_598006.1:n.1983-78_1983-65delinsTTCCCCCTTCCTCC