Canonical Allele Identifier: CA344255681
Gene: SYT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596790C>A , CM000663.2:g.202596790C>A GRCh38
NC_000001.10:g.202565918C>A , CM000663.1:g.202565918C>A GRCh37
NC_000001.9:g.200832541C>A NCBI36
NG_041776.1:g.118634G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1227G>T MANE Select ENSP00000356237.4:p.Glu409Asp
ENST00000367267.5:c.1227G>T ENSP00000356236.1:p.Glu409Asp
ENST00000367268.4:c.1227G>T ENSP00000356237.4:p.Glu409Asp
NM_001136504.1:c.1227G>T NP_001129976.1:p.Glu409Asp
NM_177402.4:c.1227G>T NP_796376.2:p.Glu409Asp
XM_011509192.1:c.1236G>T XP_011507494.1:p.Glu412Asp
XM_011509192.2:c.1236G>T XP_011507494.1:p.Glu412Asp
XM_017000309.2:c.1407G>T XP_016855798.1:p.Glu469Asp
XM_017000310.2:c.1398G>T XP_016855799.1:p.Glu466Asp
XM_017000311.2:c.1236G>T XP_016855800.1:p.Glu412Asp
XM_017000312.1:c.1236G>T XP_016855801.1:p.Glu412Asp
XM_017000313.1:c.1227G>T XP_016855802.1:p.Glu409Asp
NM_177402.5:c.1227G>T MANE Select NP_796376.2:p.Glu409Asp