Canonical Allele Identifier: CA36424072
Community Standard Title: NM_015375.3(DSTYK):c.2349G>T (p.Val783=)
Gene: DSTYK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205157276C>A , CM000663.2:g.205157276C>A GRCh38
NC_000001.10:g.205126404C>A , CM000663.1:g.205126404C>A GRCh37
NC_000001.9:g.203393027C>A NCBI36
NG_033904.1:g.59324G>T

Transcript Alleles

HGVS Amino-acid Change
NM_015375.3:c.2349G>T MANE Select NP_056190.1:p.Val783=
ENST00000367162.8:c.2349G>T MANE Select ENSP00000356130.3:p.Val783=
NM_015375.2:c.2349G>T NP_056190.1:p.Val783=
NM_199462.2:c.2349G>T NP_955749.1:p.Val783=
NM_199462.3:c.2349G>T NP_955749.1:p.Val783=
ENST00000367161.7:c.2349G>T ENSP00000356129.3:p.Val783=
ENST00000367162.7:c.2349G>T ENSP00000356130.3:p.Val783=
XM_011509392.1:c.2322G>T XP_011507694.1:p.Val774=
XM_011509392.2:c.2322G>T XP_011507694.1:p.Val774=
XM_011509393.1:c.1764G>T XP_011507695.1:p.Val588=
XM_011509393.2:c.1764G>T XP_011507695.1:p.Val588=
XM_011509394.1:c.1722G>T XP_011507696.1:p.Val574=
XM_011509394.2:c.1722G>T XP_011507696.1:p.Val574=