Canonical Allele Identifier: CA344397914
Community Standard Title: NM_015375.3(DSTYK):c.1384C>T (p.Arg462Ter)
Gene: DSTYK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205163896G>A , CM000663.2:g.205163896G>A GRCh38
NC_000001.10:g.205133024G>A , CM000663.1:g.205133024G>A GRCh37
NC_000001.9:g.203399647G>A NCBI36
NG_033904.1:g.52704C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015375.3:c.1384C>T MANE Select NP_056190.1:p.Arg462Ter
ENST00000367162.8:c.1384C>T MANE Select ENSP00000356130.3:p.Arg462Ter
NM_015375.2:c.1384C>T NP_056190.1:p.Arg462Ter
NM_199462.2:c.1384C>T NP_955749.1:p.Arg462Ter
NM_199462.3:c.1384C>T NP_955749.1:p.Arg462Ter
ENST00000367161.7:c.1384C>T ENSP00000356129.3:p.Arg462Ter
ENST00000367162.7:c.1384C>T ENSP00000356130.3:p.Arg462Ter
ENST00000615388.1:c.-89-145C>T ENSP00000478016.1:n.-89-145C>T
XM_011509392.1:c.1357C>T XP_011507694.1:p.Arg453Ter
XM_011509392.2:c.1357C>T XP_011507694.1:p.Arg453Ter
XM_011509393.1:c.799C>T XP_011507695.1:p.Arg267Ter
XM_011509393.2:c.799C>T XP_011507695.1:p.Arg267Ter
XM_011509394.1:c.757C>T XP_011507696.1:p.Arg253Ter
XM_011509394.2:c.757C>T XP_011507696.1:p.Arg253Ter