Canonical Allele Identifier: CA2481403130
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596837T= , CM000663.2:g.202596837T= GRCh38
NC_000001.10:g.202565965T= , CM000663.1:g.202565965T= GRCh37
NC_000001.9:g.200832588T= NCBI36
NG_041776.1:g.118587A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367268.5:c.1180A= MANE Select ENSP00000356237.4:p.Asn394=
ENST00000367267.5:c.1180A= ENSP00000356236.1:p.Asn394=
ENST00000367268.4:c.1180A= ENSP00000356237.4:p.Asn394=
NM_001136504.1:c.1180A= NP_001129976.1:p.Asn394=
NM_177402.4:c.1180A= NP_796376.2:p.Asn394=
XM_011509192.1:c.1189A= XP_011507494.1:p.Asn397=
XM_011509192.2:c.1189A= XP_011507494.1:p.Asn397=
XM_017000309.2:c.1360A= XP_016855798.1:p.Asn454=
XM_017000310.2:c.1351A= XP_016855799.1:p.Asn451=
XM_017000311.2:c.1189A= XP_016855800.1:p.Asn397=
XM_017000312.1:c.1189A= XP_016855801.1:p.Asn397=
XM_017000313.1:c.1180A= XP_016855802.1:p.Asn394=
NM_177402.5:c.1180A= MANE Select NP_796376.2:p.Asn394=