Canonical Allele Identifier: CA2481403158
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596936C= , CM000663.2:g.202596936C= GRCh38
NC_000001.10:g.202566064C= , CM000663.1:g.202566064C= GRCh37
NC_000001.9:g.200832687C= NCBI36
NG_041776.1:g.118488G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367268.5:c.1081G= MANE Select ENSP00000356237.4:p.Asp361=
ENST00000367267.5:c.1081G= ENSP00000356236.1:p.Asp361=
ENST00000367268.4:c.1081G= ENSP00000356237.4:p.Asp361=
NM_001136504.1:c.1081G= NP_001129976.1:p.Asp361=
NM_177402.4:c.1081G= NP_796376.2:p.Asp361=
XM_011509192.1:c.1090G= XP_011507494.1:p.Asp364=
XM_011509192.2:c.1090G= XP_011507494.1:p.Asp364=
XM_017000309.2:c.1261G= XP_016855798.1:p.Asp421=
XM_017000310.2:c.1252G= XP_016855799.1:p.Asp418=
XM_017000311.2:c.1090G= XP_016855800.1:p.Asp364=
XM_017000312.1:c.1090G= XP_016855801.1:p.Asp364=
XM_017000313.1:c.1081G= XP_016855802.1:p.Asp361=
NM_177402.5:c.1081G= MANE Select NP_796376.2:p.Asp361=