Canonical Allele Identifier: CA2573981620

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596933del , CM000663.2:g.202596933del	GRCh38
NC_000001.10:g.202566061del , CM000663.1:g.202566061del	GRCh37
NC_000001.9:g.200832684del	NCBI36
NG_041776.1:g.118491del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367268.5:c.1084del MANE Select	ENSP00000356237.4:p.Tyr362MetfsTer10
ENST00000367267.5:c.1084del	ENSP00000356236.1:p.Tyr362MetfsTer10
ENST00000367268.4:c.1084del	ENSP00000356237.4:p.Tyr362MetfsTer10
NM_001136504.1:c.1084del	NP_001129976.1:p.Tyr362MetfsTer10
NM_177402.4:c.1084del	NP_796376.2:p.Tyr362MetfsTer10
XM_011509192.1:c.1093del	XP_011507494.1:p.Tyr365MetfsTer10
XM_011509192.2:c.1093del	XP_011507494.1:p.Tyr365MetfsTer10
XM_017000309.2:c.1264del	XP_016855798.1:p.Tyr422MetfsTer10
XM_017000310.2:c.1255del	XP_016855799.1:p.Tyr419MetfsTer10
XM_017000311.2:c.1093del	XP_016855800.1:p.Tyr365MetfsTer10
XM_017000312.1:c.1093del	XP_016855801.1:p.Tyr365MetfsTer10
XM_017000313.1:c.1084del	XP_016855802.1:p.Tyr362MetfsTer10
NM_177402.5:c.1084del MANE Select	NP_796376.2:p.Tyr362MetfsTer10