Canonical Allele Identifier: CA344401119

Gene: DSTYK

Linked Data

• MyVariant Identifiers: chr1:g.205138571G>T (hg19) ; chr1:g.205169443G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205169443G>T , CM000663.2:g.205169443G>T	GRCh38
NC_000001.10:g.205138571G>T , CM000663.1:g.205138571G>T	GRCh37
NC_000001.9:g.203405194G>T	NCBI36
NG_033904.1:g.47157C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367162.8:c.1044C>A MANE Select	ENSP00000356130.3:p.His348Gln
ENST00000367161.7:c.1044C>A	ENSP00000356129.3:p.His348Gln
ENST00000367162.7:c.1044C>A	ENSP00000356130.3:p.His348Gln
ENST00000615388.1:c.-90+3594C>A	ENSP00000478016.1:n.-90+3594C>A
NM_015375.2:c.1044C>A	NP_056190.1:p.His348Gln
NM_199462.2:c.1044C>A	NP_955749.1:p.His348Gln
XM_011509392.1:c.1017C>A	XP_011507694.1:p.His339Gln
XM_011509393.1:c.459C>A	XP_011507695.1:p.His153Gln
XM_011509394.1:c.417C>A	XP_011507696.1:p.His139Gln
XM_011509392.2:c.1017C>A	XP_011507694.1:p.His339Gln
XM_011509393.2:c.459C>A	XP_011507695.1:p.His153Gln
XM_011509394.2:c.417C>A	XP_011507696.1:p.His139Gln
NM_015375.3:c.1044C>A MANE Select	NP_056190.1:p.His348Gln
NM_199462.3:c.1044C>A	NP_955749.1:p.His348Gln