Canonical Allele Identifier: CA2481403122

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596822T= , CM000663.2:g.202596822T=	GRCh38
NC_000001.10:g.202565950T= , CM000663.1:g.202565950T=	GRCh37
NC_000001.9:g.200832573T=	NCBI36
NG_041776.1:g.118602A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1195A= MANE Select	ENSP00000356237.4:p.Ile399=
ENST00000367267.5:c.1195A=	ENSP00000356236.1:p.Ile399=
ENST00000367268.4:c.1195A=	ENSP00000356237.4:p.Ile399=
NM_001136504.1:c.1195A=	NP_001129976.1:p.Ile399=
NM_177402.4:c.1195A=	NP_796376.2:p.Ile399=
XM_011509192.1:c.1204A=	XP_011507494.1:p.Ile402=
XM_011509192.2:c.1204A=	XP_011507494.1:p.Ile402=
XM_017000309.2:c.1375A=	XP_016855798.1:p.Ile459=
XM_017000310.2:c.1366A=	XP_016855799.1:p.Ile456=
XM_017000311.2:c.1204A=	XP_016855800.1:p.Ile402=
XM_017000312.1:c.1204A=	XP_016855801.1:p.Ile402=
XM_017000313.1:c.1195A=	XP_016855802.1:p.Ile399=
NM_177402.5:c.1195A= MANE Select	NP_796376.2:p.Ile399=