Canonical Allele Identifier: CA2481403196

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597021_202597022delinsAT , CM000663.2:g.202597021_202597022delinsAT	GRCh38
NC_000001.10:g.202566149_202566150delinsAT , CM000663.1:g.202566149_202566150delinsAT	GRCh37
NC_000001.9:g.200832772_200832773delinsAT	NCBI36
NG_041776.1:g.118402_118403delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-59_1054-58delinsAT MANE Select	ENSP00000356237.4:n.1054-59_1054-58delinsAT
ENST00000367267.5:c.1054-59_1054-58delinsAT	ENSP00000356236.1:n.1054-59_1054-58delinsAT
ENST00000367268.4:c.1054-59_1054-58delinsAT	ENSP00000356237.4:n.1054-59_1054-58delinsAT
NM_001136504.1:c.1054-59_1054-58delinsAT	NP_001129976.1:n.1054-59_1054-58delinsAT
NM_177402.4:c.1054-59_1054-58delinsAT	NP_796376.2:n.1054-59_1054-58delinsAT
XM_011509192.1:c.1063-59_1063-58delinsAT	XP_011507494.1:n.1063-59_1063-58delinsAT
XR_922430.1:n.45_46delinsAT
XM_011509192.2:c.1063-59_1063-58delinsAT	XP_011507494.1:n.1063-59_1063-58delinsAT
XM_017000309.2:c.1234-59_1234-58delinsAT	XP_016855798.1:n.1234-59_1234-58delinsAT
XM_017000310.2:c.1225-59_1225-58delinsAT	XP_016855799.1:n.1225-59_1225-58delinsAT
XM_017000311.2:c.1063-59_1063-58delinsAT	XP_016855800.1:n.1063-59_1063-58delinsAT
XM_017000312.1:c.1063-59_1063-58delinsAT	XP_016855801.1:n.1063-59_1063-58delinsAT
XM_017000313.1:c.1054-59_1054-58delinsAT	XP_016855802.1:n.1054-59_1054-58delinsAT
NM_177402.5:c.1054-59_1054-58delinsAT MANE Select	NP_796376.2:n.1054-59_1054-58delinsAT