Canonical Allele Identifier: CA2481403267

Gene: SYT2

Linked Data

• dbSNP Id: rs1690331065

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597220_202597224del , CM000663.2:g.202597220_202597224del	GRCh38
NC_000001.10:g.202566348_202566352del , CM000663.1:g.202566348_202566352del	GRCh37
NC_000001.9:g.200832971_200832975del	NCBI36
NG_041776.1:g.118203_118207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-258_1054-254del MANE Select	ENSP00000356237.4:n.1054-258_1054-254del
ENST00000367267.5:c.1054-258_1054-254del	ENSP00000356236.1:n.1054-258_1054-254del
ENST00000367268.4:c.1054-258_1054-254del	ENSP00000356237.4:n.1054-258_1054-254del
NM_001136504.1:c.1054-258_1054-254del	NP_001129976.1:n.1054-258_1054-254del
NM_177402.4:c.1054-258_1054-254del	NP_796376.2:n.1054-258_1054-254del
XM_011509192.1:c.1063-258_1063-254del	XP_011507494.1:n.1063-258_1063-254del
XR_922430.1:n.84+160_84+164del
XM_011509192.2:c.1063-258_1063-254del	XP_011507494.1:n.1063-258_1063-254del
XM_017000309.2:c.1234-258_1234-254del	XP_016855798.1:n.1234-258_1234-254del
XM_017000310.2:c.1225-258_1225-254del	XP_016855799.1:n.1225-258_1225-254del
XM_017000311.2:c.1063-258_1063-254del	XP_016855800.1:n.1063-258_1063-254del
XM_017000312.1:c.1063-258_1063-254del	XP_016855801.1:n.1063-258_1063-254del
XM_017000313.1:c.1054-258_1054-254del	XP_016855802.1:n.1054-258_1054-254del
NM_177402.5:c.1054-258_1054-254del MANE Select	NP_796376.2:n.1054-258_1054-254del