Canonical Allele Identifier: CA2481403123

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596822_202596834delinsTGGGCCTCCGGGG , CM000663.2:g.202596822_202596834delinsTGGGCCTCCGGGG	GRCh38
NC_000001.10:g.202565950_202565962delinsTGGGCCTCCGGGG , CM000663.1:g.202565950_202565962delinsTGGGCCTCCGGGG	GRCh37
NC_000001.9:g.200832573_200832585delinsTGGGCCTCCGGGG	NCBI36
NG_041776.1:g.118590_118602delinsCCCCGGAGGCCCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367268.5:c.1183_1195delinsCCCCGGAGGCCCA MANE Select	ENSP00000356237.4:p.Pro395=
ENST00000367267.5:c.1183_1195delinsCCCCGGAGGCCCA	ENSP00000356236.1:p.Pro395=
ENST00000367268.4:c.1183_1195delinsCCCCGGAGGCCCA	ENSP00000356237.4:p.Pro395=
NM_001136504.1:c.1183_1195delinsCCCCGGAGGCCCA	NP_001129976.1:p.Pro395=
NM_177402.4:c.1183_1195delinsCCCCGGAGGCCCA	NP_796376.2:p.Pro395=
XM_011509192.1:c.1192_1204delinsCCCCGGAGGCCCA	XP_011507494.1:p.Pro398=
XM_011509192.2:c.1192_1204delinsCCCCGGAGGCCCA	XP_011507494.1:p.Pro398=
XM_017000309.2:c.1363_1375delinsCCCCGGAGGCCCA	XP_016855798.1:p.Pro455=
XM_017000310.2:c.1354_1366delinsCCCCGGAGGCCCA	XP_016855799.1:p.Pro452=
XM_017000311.2:c.1192_1204delinsCCCCGGAGGCCCA	XP_016855800.1:p.Pro398=
XM_017000312.1:c.1192_1204delinsCCCCGGAGGCCCA	XP_016855801.1:p.Pro398=
XM_017000313.1:c.1183_1195delinsCCCCGGAGGCCCA	XP_016855802.1:p.Pro395=
NM_177402.5:c.1183_1195delinsCCCCGGAGGCCCA MANE Select	NP_796376.2:p.Pro395=