Canonical Allele Identifier: CA344397395
Community Standard Title: NM_015375.3(DSTYK):c.1477G>T (p.Gly493Ter)
Gene: DSTYK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205163803C>A , CM000663.2:g.205163803C>A GRCh38
NC_000001.10:g.205132931C>A , CM000663.1:g.205132931C>A GRCh37
NC_000001.9:g.203399554C>A NCBI36
NG_033904.1:g.52797G>T

Transcript Alleles

HGVS Amino-acid Change
NM_015375.3:c.1477G>T MANE Select NP_056190.1:p.Gly493Ter
ENST00000367162.8:c.1477G>T MANE Select ENSP00000356130.3:p.Gly493Ter
NM_015375.2:c.1477G>T NP_056190.1:p.Gly493Ter
NM_199462.2:c.1477G>T NP_955749.1:p.Gly493Ter
NM_199462.3:c.1477G>T NP_955749.1:p.Gly493Ter
ENST00000367161.7:c.1477G>T ENSP00000356129.3:p.Gly493Ter
ENST00000367162.7:c.1477G>T ENSP00000356130.3:p.Gly493Ter
ENST00000615388.1:c.-89-52G>T ENSP00000478016.1:n.-89-52G>T
XM_011509392.1:c.1450G>T XP_011507694.1:p.Gly484Ter
XM_011509392.2:c.1450G>T XP_011507694.1:p.Gly484Ter
XM_011509393.1:c.892G>T XP_011507695.1:p.Gly298Ter
XM_011509393.2:c.892G>T XP_011507695.1:p.Gly298Ter
XM_011509394.1:c.850G>T XP_011507696.1:p.Gly284Ter
XM_011509394.2:c.850G>T XP_011507696.1:p.Gly284Ter