Canonical Allele Identifier: CA2993663738

Gene: DSTYK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205169085A>T , CM000663.2:g.205169085A>T	GRCh38
NC_000001.10:g.205138213A>T , CM000663.1:g.205138213A>T	GRCh37
NC_000001.9:g.203404836A>T	NCBI36
NG_033904.1:g.47515T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015375.3:c.1324+78T>A MANE Select	NP_056190.1:n.1324+78T>A
ENST00000367162.8:c.1324+78T>A MANE Select	ENSP00000356130.3:n.1324+78T>A
NM_015375.2:c.1324+78T>A	NP_056190.1:n.1324+78T>A
NM_199462.2:c.1324+78T>A	NP_955749.1:n.1324+78T>A
NM_199462.3:c.1324+78T>A	NP_955749.1:n.1324+78T>A
ENST00000367161.7:c.1324+78T>A	ENSP00000356129.3:n.1324+78T>A
ENST00000367162.7:c.1324+78T>A	ENSP00000356130.3:n.1324+78T>A
ENST00000615388.1:c.-90+3952T>A	ENSP00000478016.1:n.-90+3952T>A
XM_011509392.1:c.1297+78T>A	XP_011507694.1:n.1297+78T>A
XM_011509392.2:c.1297+78T>A	XP_011507694.1:n.1297+78T>A
XM_011509393.1:c.739+78T>A	XP_011507695.1:n.739+78T>A
XM_011509393.2:c.739+78T>A	XP_011507695.1:n.739+78T>A
XM_011509394.1:c.697+78T>A	XP_011507696.1:n.697+78T>A
XM_011509394.2:c.697+78T>A	XP_011507696.1:n.697+78T>A