Canonical Allele Identifier: CA2573990503

Gene: DSTYK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205159691G>T , CM000663.2:g.205159691G>T	GRCh38
NC_000001.10:g.205128819G>T , CM000663.1:g.205128819G>T	GRCh37
NC_000001.9:g.203395442G>T	NCBI36
NG_033904.1:g.56909C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015375.3:c.2106-12C>A MANE Select	NP_056190.1:n.2106-12C>A
ENST00000367162.8:c.2106-12C>A MANE Select	ENSP00000356130.3:n.2106-12C>A
NM_015375.2:c.2106-12C>A	NP_056190.1:n.2106-12C>A
NM_199462.2:c.2106-12C>A	NP_955749.1:n.2106-12C>A
NM_199462.3:c.2106-12C>A	NP_955749.1:n.2106-12C>A
ENST00000367161.7:c.2106-12C>A	ENSP00000356129.3:n.2106-12C>A
ENST00000367162.7:c.2106-12C>A	ENSP00000356130.3:n.2106-12C>A
XM_011509392.1:c.2079-12C>A	XP_011507694.1:n.2079-12C>A
XM_011509392.2:c.2079-12C>A	XP_011507694.1:n.2079-12C>A
XM_011509393.1:c.1521-12C>A	XP_011507695.1:n.1521-12C>A
XM_011509393.2:c.1521-12C>A	XP_011507695.1:n.1521-12C>A
XM_011509394.1:c.1479-12C>A	XP_011507696.1:n.1479-12C>A
XM_011509394.2:c.1479-12C>A	XP_011507696.1:n.1479-12C>A