Canonical Allele Identifier: CA2649903300

Gene: SYT2

Linked Data

• gnomAD v4: 1-202596849-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596851dup , CM000663.2:g.202596851dup	GRCh38
NC_000001.10:g.202565979dup , CM000663.1:g.202565979dup	GRCh37
NC_000001.9:g.200832602dup	NCBI36
NG_041776.1:g.118574dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1167dup MANE Select	ENSP00000356237.4:p.Asp390ArgfsTer19
ENST00000367267.5:c.1167dup	ENSP00000356236.1:p.Asp390ArgfsTer19
ENST00000367268.4:c.1167dup	ENSP00000356237.4:p.Asp390ArgfsTer19
NM_001136504.1:c.1167dup	NP_001129976.1:p.Asp390ArgfsTer19
NM_177402.4:c.1167dup	NP_796376.2:p.Asp390ArgfsTer19
XM_011509192.1:c.1176dup	XP_011507494.1:p.Asp393ArgfsTer19
XM_011509192.2:c.1176dup	XP_011507494.1:p.Asp393ArgfsTer19
XM_017000309.2:c.1347dup	XP_016855798.1:p.Asp450ArgfsTer19
XM_017000310.2:c.1338dup	XP_016855799.1:p.Asp447ArgfsTer19
XM_017000311.2:c.1176dup	XP_016855800.1:p.Asp393ArgfsTer19
XM_017000312.1:c.1176dup	XP_016855801.1:p.Asp393ArgfsTer19
XM_017000313.1:c.1167dup	XP_016855802.1:p.Asp390ArgfsTer19
NM_177402.5:c.1167dup MANE Select	NP_796376.2:p.Asp390ArgfsTer19