Canonical Allele Identifier: CA1143910181

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596850G= , CM000663.2:g.202596850G=	GRCh38
NC_000001.10:g.202565978G= , CM000663.1:g.202565978G=	GRCh37
NC_000001.9:g.200832601G=	NCBI36
NG_041776.1:g.118574C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1167C= MANE Select	ENSP00000356237.4:p.Ser389=
ENST00000367267.5:c.1167C=	ENSP00000356236.1:p.Ser389=
ENST00000367268.4:c.1167C=	ENSP00000356237.4:p.Ser389=
NM_001136504.1:c.1167C=	NP_001129976.1:p.Ser389=
NM_177402.4:c.1167C=	NP_796376.2:p.Ser389=
XM_011509192.1:c.1176C=	XP_011507494.1:p.Ser392=
XM_011509192.2:c.1176C=	XP_011507494.1:p.Ser392=
XM_017000309.2:c.1347C=	XP_016855798.1:p.Ser449=
XM_017000310.2:c.1338C=	XP_016855799.1:p.Ser446=
XM_017000311.2:c.1176C=	XP_016855800.1:p.Ser392=
XM_017000312.1:c.1176C=	XP_016855801.1:p.Ser392=
XM_017000313.1:c.1167C=	XP_016855802.1:p.Ser389=
NM_177402.5:c.1167C= MANE Select	NP_796376.2:p.Ser389=