Canonical Allele Identifier: CA2481403266

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597216_202597221delinsGGAGAA , CM000663.2:g.202597216_202597221delinsGGAGAA	GRCh38
NC_000001.10:g.202566344_202566349delinsGGAGAA , CM000663.1:g.202566344_202566349delinsGGAGAA	GRCh37
NC_000001.9:g.200832967_200832972delinsGGAGAA	NCBI36
NG_041776.1:g.118203_118208delinsTTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-258_1054-253delinsTTCTCC MANE Select	ENSP00000356237.4:n.1054-258_1054-253delinsTTCTCC
ENST00000367267.5:c.1054-258_1054-253delinsTTCTCC	ENSP00000356236.1:n.1054-258_1054-253delinsTTCTCC
ENST00000367268.4:c.1054-258_1054-253delinsTTCTCC	ENSP00000356237.4:n.1054-258_1054-253delinsTTCTCC
NM_001136504.1:c.1054-258_1054-253delinsTTCTCC	NP_001129976.1:n.1054-258_1054-253delinsTTCTCC
NM_177402.4:c.1054-258_1054-253delinsTTCTCC	NP_796376.2:n.1054-258_1054-253delinsTTCTCC
XM_011509192.1:c.1063-258_1063-253delinsTTCTCC	XP_011507494.1:n.1063-258_1063-253delinsTTCTCC
XR_922430.1:n.84+156_84+161delinsGGAGAA
XM_011509192.2:c.1063-258_1063-253delinsTTCTCC	XP_011507494.1:n.1063-258_1063-253delinsTTCTCC
XM_017000309.2:c.1234-258_1234-253delinsTTCTCC	XP_016855798.1:n.1234-258_1234-253delinsTTCTCC
XM_017000310.2:c.1225-258_1225-253delinsTTCTCC	XP_016855799.1:n.1225-258_1225-253delinsTTCTCC
XM_017000311.2:c.1063-258_1063-253delinsTTCTCC	XP_016855800.1:n.1063-258_1063-253delinsTTCTCC
XM_017000312.1:c.1063-258_1063-253delinsTTCTCC	XP_016855801.1:n.1063-258_1063-253delinsTTCTCC
XM_017000313.1:c.1054-258_1054-253delinsTTCTCC	XP_016855802.1:n.1054-258_1054-253delinsTTCTCC
NM_177402.5:c.1054-258_1054-253delinsTTCTCC MANE Select	NP_796376.2:n.1054-258_1054-253delinsTTCTCC