Canonical Allele Identifier: CA14674281

Gene: ZNF536

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.30608983A>G , CM000681.2:g.30608983A>G	GRCh38
NC_000019.9:g.31099890A>G , CM000681.1:g.31099890A>G	GRCh37
NC_000019.8:g.35791730A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592773.3:c.3895+59469A>G	ENSP00000467909.3:n.3895+59469A>G
ENST00000706143.1:c.1648+59469A>G	ENSP00000516227.1:n.1648+59469A>G
ENST00000706147.1:c.2323+73984A>G	ENSP00000516230.1:n.2323+73984A>G
ENST00000706148.1:c.3896-34554A>G	ENSP00000516231.1:n.3896-34554A>G
ENST00000706149.1:c.1648+59469A>G	ENSP00000516232.1:n.1648+59469A>G
ENST00000706150.1:c.3896-34554A>G	ENSP00000516233.1:n.3896-34554A>G
ENST00000592773.2:c.169+59469A>G	ENSP00000467909.2:n.169+59469A>G
XM_011527554.1:c.3982+59469A>G	XP_011525856.1:n.3982+59469A>G
XM_011527555.1:c.3982+59469A>G	XP_011525857.1:n.3982+59469A>G
XM_011527556.1:c.3982+59469A>G	XP_011525858.1:n.3982+59469A>G
XM_011527557.1:c.3982+59469A>G	XP_011525859.1:n.3982+59469A>G
XM_011527558.1:c.3982+59469A>G	XP_011525860.1:n.3982+59469A>G
XM_011527559.1:c.3964+59469A>G	XP_011525861.1:n.3964+59469A>G
XM_011527560.1:c.3895+59469A>G	XP_011525862.1:n.3895+59469A>G
NM_001352260.1:c.3896-34554A>G	NP_001339189.1:n.3896-34554A>G
XM_011527554.2:c.3982+59469A>G	XP_011525856.1:n.3982+59469A>G
XM_011527555.2:c.3982+59469A>G	XP_011525857.1:n.3982+59469A>G
XM_011527557.2:c.3982+59469A>G	XP_011525859.1:n.3982+59469A>G
XM_011527558.2:c.3982+59469A>G	XP_011525860.1:n.3982+59469A>G
XM_011527560.2:c.3895+59469A>G	XP_011525862.1:n.3895+59469A>G
XM_017027527.1:c.3982+59469A>G	XP_016883016.1:n.3982+59469A>G
XM_017027528.1:c.3982+59469A>G	XP_016883017.1:n.3982+59469A>G
XM_017027529.1:c.3982+59469A>G	XP_016883018.1:n.3982+59469A>G
XM_017027530.1:c.3982+59469A>G	XP_016883019.1:n.3982+59469A>G
XM_017027531.1:c.3982+59469A>G	XP_016883020.1:n.3982+59469A>G
XM_017027532.1:c.3982+59469A>G	XP_016883021.1:n.3982+59469A>G
XM_017027533.1:c.3982+59469A>G	XP_016883022.1:n.3982+59469A>G
XM_017027534.1:c.3982+59469A>G	XP_016883023.1:n.3982+59469A>G
XM_017027535.1:c.3982+59469A>G	XP_016883024.1:n.3982+59469A>G
XM_017027536.1:c.3982+59469A>G	XP_016883025.1:n.3982+59469A>G
XM_017027537.1:c.3895+59469A>G	XP_016883026.1:n.3895+59469A>G
XM_017027538.1:c.3983-34554A>G	XP_016883027.1:n.3983-34554A>G
XM_017027540.1:c.3896-34554A>G	XP_016883029.1:n.3896-34554A>G
XM_017027543.2:c.1849+59469A>G	XP_016883032.1:n.1849+59469A>G
XM_024451807.1:c.3982+59469A>G	XP_024307575.1:n.3982+59469A>G
NM_001352260.2:c.3896-34554A>G	NP_001339189.1:n.3896-34554A>G
NM_001376110.1:c.3895+59469A>G	NP_001363039.1:n.3895+59469A>G
NM_001376111.1:c.3895+59469A>G	NP_001363040.1:n.3895+59469A>G