Canonical Allele Identifier: CA344255577
Gene: SYT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596762T>A , CM000663.2:g.202596762T>A GRCh38
NC_000001.10:g.202565890T>A , CM000663.1:g.202565890T>A GRCh37
NC_000001.9:g.200832513T>A NCBI36
NG_041776.1:g.118662A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1255A>T MANE Select ENSP00000356237.4:p.Lys419Ter
ENST00000367267.5:c.1255A>T ENSP00000356236.1:p.Lys419Ter
ENST00000367268.4:c.1255A>T ENSP00000356237.4:p.Lys419Ter
NM_001136504.1:c.1255A>T NP_001129976.1:p.Lys419Ter
NM_177402.4:c.1255A>T NP_796376.2:p.Lys419Ter
XM_011509192.1:c.1264A>T XP_011507494.1:p.Lys422Ter
XM_011509192.2:c.1264A>T XP_011507494.1:p.Lys422Ter
XM_017000309.2:c.1435A>T XP_016855798.1:p.Lys479Ter
XM_017000310.2:c.1426A>T XP_016855799.1:p.Lys476Ter
XM_017000311.2:c.1264A>T XP_016855800.1:p.Lys422Ter
XM_017000312.1:c.1264A>T XP_016855801.1:p.Lys422Ter
XM_017000313.1:c.1255A>T XP_016855802.1:p.Lys419Ter
NM_177402.5:c.1255A>T MANE Select NP_796376.2:p.Lys419Ter