Canonical Allele Identifier: CA2481403188

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202596999_202597014delinsAGACGTGGGATCCCAT , CM000663.2:g.202596999_202597014delinsAGACGTGGGATCCCAT	GRCh38
NC_000001.10:g.202566127_202566142delinsAGACGTGGGATCCCAT , CM000663.1:g.202566127_202566142delinsAGACGTGGGATCCCAT	GRCh37
NC_000001.9:g.200832750_200832765delinsAGACGTGGGATCCCAT	NCBI36
NG_041776.1:g.118410_118425delinsATGGGATCCCACGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-51_1054-36delinsATGGGATCCCACGTCT MANE Select	ENSP00000356237.4:n.1054-51_1054-36delinsATGGGATCCCACGTCT
ENST00000367267.5:c.1054-51_1054-36delinsATGGGATCCCACGTCT	ENSP00000356236.1:n.1054-51_1054-36delinsATGGGATCCCACGTCT
ENST00000367268.4:c.1054-51_1054-36delinsATGGGATCCCACGTCT	ENSP00000356237.4:n.1054-51_1054-36delinsATGGGATCCCACGTCT
NM_001136504.1:c.1054-51_1054-36delinsATGGGATCCCACGTCT	NP_001129976.1:n.1054-51_1054-36delinsATGGGATCCCACGTCT
NM_177402.4:c.1054-51_1054-36delinsATGGGATCCCACGTCT	NP_796376.2:n.1054-51_1054-36delinsATGGGATCCCACGTCT
XM_011509192.1:c.1063-51_1063-36delinsATGGGATCCCACGTCT	XP_011507494.1:n.1063-51_1063-36delinsATGGGATCCCACGTCT
XR_922430.1:n.23_38delinsAGACGTGGGATCCCAT
XM_011509192.2:c.1063-51_1063-36delinsATGGGATCCCACGTCT	XP_011507494.1:n.1063-51_1063-36delinsATGGGATCCCACGTCT
XM_017000309.2:c.1234-51_1234-36delinsATGGGATCCCACGTCT	XP_016855798.1:n.1234-51_1234-36delinsATGGGATCCCACGTCT
XM_017000310.2:c.1225-51_1225-36delinsATGGGATCCCACGTCT	XP_016855799.1:n.1225-51_1225-36delinsATGGGATCCCACGTCT
XM_017000311.2:c.1063-51_1063-36delinsATGGGATCCCACGTCT	XP_016855800.1:n.1063-51_1063-36delinsATGGGATCCCACGTCT
XM_017000312.1:c.1063-51_1063-36delinsATGGGATCCCACGTCT	XP_016855801.1:n.1063-51_1063-36delinsATGGGATCCCACGTCT
XM_017000313.1:c.1054-51_1054-36delinsATGGGATCCCACGTCT	XP_016855802.1:n.1054-51_1054-36delinsATGGGATCCCACGTCT
NM_177402.5:c.1054-51_1054-36delinsATGGGATCCCACGTCT MANE Select	NP_796376.2:n.1054-51_1054-36delinsATGGGATCCCACGTCT