Canonical Allele Identifier: CA1352732

Gene: DSTYK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205161390G>A , CM000663.2:g.205161390G>A	GRCh38
NC_000001.10:g.205130518G>A , CM000663.1:g.205130518G>A	GRCh37
NC_000001.9:g.203397141G>A	NCBI36
NG_033904.1:g.55210C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015375.3:c.1819-3C>T MANE Select	NP_056190.1:n.1819-3C>T
ENST00000367162.8:c.1819-3C>T MANE Select	ENSP00000356130.3:n.1819-3C>T
NM_015375.2:c.1819-3C>T	NP_056190.1:n.1819-3C>T
NM_199462.2:c.1819-3C>T	NP_955749.1:n.1819-3C>T
NM_199462.3:c.1819-3C>T	NP_955749.1:n.1819-3C>T
ENST00000367161.7:c.1819-3C>T	ENSP00000356129.3:n.1819-3C>T
ENST00000367162.7:c.1819-3C>T	ENSP00000356130.3:n.1819-3C>T
ENST00000615388.1:c.202-3C>T	ENSP00000478016.1:n.202-3C>T
XM_011509392.1:c.1792-3C>T	XP_011507694.1:n.1792-3C>T
XM_011509392.2:c.1792-3C>T	XP_011507694.1:n.1792-3C>T
XM_011509393.1:c.1234-3C>T	XP_011507695.1:n.1234-3C>T
XM_011509393.2:c.1234-3C>T	XP_011507695.1:n.1234-3C>T
XM_011509394.1:c.1192-3C>T	XP_011507696.1:n.1192-3C>T
XM_011509394.2:c.1192-3C>T	XP_011507696.1:n.1192-3C>T