Canonical Allele Identifier: CA344397866

Gene: DSTYK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205163886T>C , CM000663.2:g.205163886T>C	GRCh38
NC_000001.10:g.205133014T>C , CM000663.1:g.205133014T>C	GRCh37
NC_000001.9:g.203399637T>C	NCBI36
NG_033904.1:g.52714A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015375.3:c.1394A>G MANE Select	NP_056190.1:p.Gln465Arg
ENST00000367162.8:c.1394A>G MANE Select	ENSP00000356130.3:p.Gln465Arg
NM_015375.2:c.1394A>G	NP_056190.1:p.Gln465Arg
NM_199462.2:c.1394A>G	NP_955749.1:p.Gln465Arg
NM_199462.3:c.1394A>G	NP_955749.1:p.Gln465Arg
ENST00000367161.7:c.1394A>G	ENSP00000356129.3:p.Gln465Arg
ENST00000367162.7:c.1394A>G	ENSP00000356130.3:p.Gln465Arg
ENST00000615388.1:c.-89-135A>G	ENSP00000478016.1:n.-89-135A>G
XM_011509392.1:c.1367A>G	XP_011507694.1:p.Gln456Arg
XM_011509392.2:c.1367A>G	XP_011507694.1:p.Gln456Arg
XM_011509393.1:c.809A>G	XP_011507695.1:p.Gln270Arg
XM_011509393.2:c.809A>G	XP_011507695.1:p.Gln270Arg
XM_011509394.1:c.767A>G	XP_011507696.1:p.Gln256Arg
XM_011509394.2:c.767A>G	XP_011507696.1:p.Gln256Arg