Canonical Allele Identifier: CA9353508

Gene: ZNF536

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.30534879G>A , CM000681.2:g.30534879G>A	GRCh38
NC_000019.9:g.31025786G>A , CM000681.1:g.31025786G>A	GRCh37
NC_000019.8:g.35717626G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592773.3:c.2203G>A	ENSP00000467909.3:p.Val735Ile
ENST00000706142.1:c.2203G>A	ENSP00000516226.1:p.Val735Ile
ENST00000706143.1:c.-45G>A	ENSP00000516227.1:n.-45G>A
ENST00000706144.1:c.2203G>A	ENSP00000516228.1:p.Val735Ile
ENST00000706145.1:n.2340G>A
ENST00000706146.1:c.2203G>A	ENSP00000516229.1:p.Val735Ile
ENST00000706147.1:c.2203G>A	ENSP00000516230.1:p.Val735Ile
ENST00000706148.1:c.2203G>A	ENSP00000516231.1:p.Val735Ile
ENST00000706149.1:c.-45G>A	ENSP00000516232.1:n.-45G>A
ENST00000706150.1:c.2203G>A	ENSP00000516233.1:p.Val735Ile
ENST00000355537.4:c.2203G>A MANE Select	ENSP00000347730.1:p.Val735Ile
ENST00000355537.3:c.2203G>A	ENSP00000347730.1:p.Val735Ile
ENST00000585628.5:c.2203G>A	ENSP00000465771.1:p.Val735Ile
NM_014717.1:c.2203G>A	NP_055532.1:p.Val735Ile
NM_014717.2:c.2203G>A	NP_055532.1:p.Val735Ile
XM_011527554.1:c.2203G>A	XP_011525856.1:p.Val735Ile
XM_011527555.1:c.2203G>A	XP_011525857.1:p.Val735Ile
XM_011527556.1:c.2203G>A	XP_011525858.1:p.Val735Ile
XM_011527557.1:c.2203G>A	XP_011525859.1:p.Val735Ile
XM_011527558.1:c.2203G>A	XP_011525860.1:p.Val735Ile
XM_011527559.1:c.2272G>A	XP_011525861.1:p.Val758Ile
XM_011527560.1:c.2203G>A	XP_011525862.1:p.Val735Ile
NM_001352260.1:c.2203G>A	NP_001339189.1:p.Val735Ile
XM_011527554.2:c.2203G>A	XP_011525856.1:p.Val735Ile
XM_011527555.2:c.2203G>A	XP_011525857.1:p.Val735Ile
XM_011527557.2:c.2203G>A	XP_011525859.1:p.Val735Ile
XM_011527558.2:c.2203G>A	XP_011525860.1:p.Val735Ile
XM_011527560.2:c.2203G>A	XP_011525862.1:p.Val735Ile
XM_017027527.1:c.2203G>A	XP_016883016.1:p.Val735Ile
XM_017027528.1:c.2203G>A	XP_016883017.1:p.Val735Ile
XM_017027529.1:c.2203G>A	XP_016883018.1:p.Val735Ile
XM_017027530.1:c.2203G>A	XP_016883019.1:p.Val735Ile
XM_017027531.1:c.2203G>A	XP_016883020.1:p.Val735Ile
XM_017027532.1:c.2203G>A	XP_016883021.1:p.Val735Ile
XM_017027533.1:c.2203G>A	XP_016883022.1:p.Val735Ile
XM_017027534.1:c.2203G>A	XP_016883023.1:p.Val735Ile
XM_017027535.1:c.2203G>A	XP_016883024.1:p.Val735Ile
XM_017027536.1:c.2203G>A	XP_016883025.1:p.Val735Ile
XM_017027537.1:c.2203G>A	XP_016883026.1:p.Val735Ile
XM_017027538.1:c.2203G>A	XP_016883027.1:p.Val735Ile
XM_017027539.1:c.2203G>A	XP_016883028.1:p.Val735Ile
XM_017027540.1:c.2203G>A	XP_016883029.1:p.Val735Ile
XM_017027542.1:c.2203G>A	XP_016883031.1:p.Val735Ile
XM_017027543.2:c.70G>A	XP_016883032.1:p.Val24Ile
XM_024451807.1:c.2203G>A	XP_024307575.1:p.Val735Ile
NM_014717.3:c.2203G>A MANE Select	NP_055532.1:p.Val735Ile
NM_001352260.2:c.2203G>A	NP_001339189.1:p.Val735Ile
NM_001376110.1:c.2203G>A	NP_001363039.1:p.Val735Ile
NM_001376111.1:c.2203G>A	NP_001363040.1:p.Val735Ile