Canonical Allele Identifier: CA2508320441

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596941del , CM000663.2:g.202596941del	GRCh38
NC_000001.10:g.202566069del , CM000663.1:g.202566069del	GRCh37
NC_000001.9:g.200832692del	NCBI36
NG_041776.1:g.118483del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367268.5:c.1076del MANE Select	ENSP00000356237.4:p.Val359GlyfsTer13
ENST00000367267.5:c.1076del	ENSP00000356236.1:p.Val359GlyfsTer13
ENST00000367268.4:c.1076del	ENSP00000356237.4:p.Val359GlyfsTer13
NM_001136504.1:c.1076del	NP_001129976.1:p.Val359GlyfsTer13
NM_177402.4:c.1076del	NP_796376.2:p.Val359GlyfsTer13
XM_011509192.1:c.1085del	XP_011507494.1:p.Val362GlyfsTer13
XM_011509192.2:c.1085del	XP_011507494.1:p.Val362GlyfsTer13
XM_017000309.2:c.1256del	XP_016855798.1:p.Val419GlyfsTer13
XM_017000310.2:c.1247del	XP_016855799.1:p.Val416GlyfsTer13
XM_017000311.2:c.1085del	XP_016855800.1:p.Val362GlyfsTer13
XM_017000312.1:c.1085del	XP_016855801.1:p.Val362GlyfsTer13
XM_017000313.1:c.1076del	XP_016855802.1:p.Val359GlyfsTer13
NM_177402.5:c.1076del MANE Select	NP_796376.2:p.Val359GlyfsTer13