Canonical Allele Identifier: CA2481403273

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597224_202597228delinsGGGAA , CM000663.2:g.202597224_202597228delinsGGGAA	GRCh38
NC_000001.10:g.202566352_202566356delinsGGGAA , CM000663.1:g.202566352_202566356delinsGGGAA	GRCh37
NC_000001.9:g.200832975_200832979delinsGGGAA	NCBI36
NG_041776.1:g.118196_118200delinsTTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-265_1054-261delinsTTCCC MANE Select	ENSP00000356237.4:n.1054-265_1054-261delinsTTCCC
ENST00000367267.5:c.1054-265_1054-261delinsTTCCC	ENSP00000356236.1:n.1054-265_1054-261delinsTTCCC
ENST00000367268.4:c.1054-265_1054-261delinsTTCCC	ENSP00000356237.4:n.1054-265_1054-261delinsTTCCC
NM_001136504.1:c.1054-265_1054-261delinsTTCCC	NP_001129976.1:n.1054-265_1054-261delinsTTCCC
NM_177402.4:c.1054-265_1054-261delinsTTCCC	NP_796376.2:n.1054-265_1054-261delinsTTCCC
XM_011509192.1:c.1063-265_1063-261delinsTTCCC	XP_011507494.1:n.1063-265_1063-261delinsTTCCC
XR_922430.1:n.84+164_84+168delinsGGGAA
XM_011509192.2:c.1063-265_1063-261delinsTTCCC	XP_011507494.1:n.1063-265_1063-261delinsTTCCC
XM_017000309.2:c.1234-265_1234-261delinsTTCCC	XP_016855798.1:n.1234-265_1234-261delinsTTCCC
XM_017000310.2:c.1225-265_1225-261delinsTTCCC	XP_016855799.1:n.1225-265_1225-261delinsTTCCC
XM_017000311.2:c.1063-265_1063-261delinsTTCCC	XP_016855800.1:n.1063-265_1063-261delinsTTCCC
XM_017000312.1:c.1063-265_1063-261delinsTTCCC	XP_016855801.1:n.1063-265_1063-261delinsTTCCC
XM_017000313.1:c.1054-265_1054-261delinsTTCCC	XP_016855802.1:n.1054-265_1054-261delinsTTCCC
NM_177402.5:c.1054-265_1054-261delinsTTCCC MANE Select	NP_796376.2:n.1054-265_1054-261delinsTTCCC