Canonical Allele Identifier: CA1352764

Gene: DSTYK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205162079C>T , CM000663.2:g.205162079C>T	GRCh38
NC_000001.10:g.205131207C>T , CM000663.1:g.205131207C>T	GRCh37
NC_000001.9:g.203397830C>T	NCBI36
NG_033904.1:g.54521G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015375.3:c.1775G>A MANE Select	NP_056190.1:p.Arg592Gln
ENST00000367162.8:c.1775G>A MANE Select	ENSP00000356130.3:p.Arg592Gln
NM_015375.2:c.1775G>A	NP_056190.1:p.Arg592Gln
NM_199462.2:c.1775G>A	NP_955749.1:p.Arg592Gln
NM_199462.3:c.1775G>A	NP_955749.1:p.Arg592Gln
ENST00000367161.7:c.1775G>A	ENSP00000356129.3:p.Arg592Gln
ENST00000367162.7:c.1775G>A	ENSP00000356130.3:p.Arg592Gln
ENST00000615388.1:c.158G>A	ENSP00000478016.1:p.Arg53Gln
XM_011509392.1:c.1748G>A	XP_011507694.1:p.Arg583Gln
XM_011509392.2:c.1748G>A	XP_011507694.1:p.Arg583Gln
XM_011509393.1:c.1190G>A	XP_011507695.1:p.Arg397Gln
XM_011509393.2:c.1190G>A	XP_011507695.1:p.Arg397Gln
XM_011509394.1:c.1148G>A	XP_011507696.1:p.Arg383Gln
XM_011509394.2:c.1148G>A	XP_011507696.1:p.Arg383Gln