Canonical Allele Identifier: CA344255828
Gene: SYT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596851G>A , CM000663.2:g.202596851G>A GRCh38
NC_000001.10:g.202565979G>A , CM000663.1:g.202565979G>A GRCh37
NC_000001.9:g.200832602G>A NCBI36
NG_041776.1:g.118573C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1166C>T MANE Select ENSP00000356237.4:p.Ser389Phe
ENST00000367267.5:c.1166C>T ENSP00000356236.1:p.Ser389Phe
ENST00000367268.4:c.1166C>T ENSP00000356237.4:p.Ser389Phe
NM_001136504.1:c.1166C>T NP_001129976.1:p.Ser389Phe
NM_177402.4:c.1166C>T NP_796376.2:p.Ser389Phe
XM_011509192.1:c.1175C>T XP_011507494.1:p.Ser392Phe
XM_011509192.2:c.1175C>T XP_011507494.1:p.Ser392Phe
XM_017000309.2:c.1346C>T XP_016855798.1:p.Ser449Phe
XM_017000310.2:c.1337C>T XP_016855799.1:p.Ser446Phe
XM_017000311.2:c.1175C>T XP_016855800.1:p.Ser392Phe
XM_017000312.1:c.1175C>T XP_016855801.1:p.Ser392Phe
XM_017000313.1:c.1166C>T XP_016855802.1:p.Ser389Phe
NM_177402.5:c.1166C>T MANE Select NP_796376.2:p.Ser389Phe