Canonical Allele Identifier: CA2747381824

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202597288_202597292del , CM000663.2:g.202597288_202597292del	GRCh38
NC_000001.10:g.202566416_202566420del , CM000663.1:g.202566416_202566420del	GRCh37
NC_000001.9:g.200833039_200833043del	NCBI36
NG_041776.1:g.118133_118137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367268.5:c.1054-328_1054-324del MANE Select	ENSP00000356237.4:n.1054-328_1054-324del
ENST00000367267.5:c.1054-328_1054-324del	ENSP00000356236.1:n.1054-328_1054-324del
ENST00000367268.4:c.1054-328_1054-324del	ENSP00000356237.4:n.1054-328_1054-324del
NM_001136504.1:c.1054-328_1054-324del	NP_001129976.1:n.1054-328_1054-324del
NM_177402.4:c.1054-328_1054-324del	NP_796376.2:n.1054-328_1054-324del
XM_011509192.1:c.1063-328_1063-324del	XP_011507494.1:n.1063-328_1063-324del
XR_922430.1:n.84+228_84+232del
XM_011509192.2:c.1063-328_1063-324del	XP_011507494.1:n.1063-328_1063-324del
XM_017000309.2:c.1234-328_1234-324del	XP_016855798.1:n.1234-328_1234-324del
XM_017000310.2:c.1225-328_1225-324del	XP_016855799.1:n.1225-328_1225-324del
XM_017000311.2:c.1063-328_1063-324del	XP_016855800.1:n.1063-328_1063-324del
XM_017000312.1:c.1063-328_1063-324del	XP_016855801.1:n.1063-328_1063-324del
XM_017000313.1:c.1054-328_1054-324del	XP_016855802.1:n.1054-328_1054-324del
NM_177402.5:c.1054-328_1054-324del MANE Select	NP_796376.2:n.1054-328_1054-324del