Canonical Allele Identifier: CA1363903178

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2001147
• ClinVar RCV Id: RCV002810958
• dbSNP Id: rs1703437440

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343031_50343041del , CM000665.2:g.50343031_50343041del	GRCh38
NC_000003.11:g.50380462_50380472del , CM000665.1:g.50380462_50380472del	GRCh37
NC_000003.10:g.50355466_50355476del	NCBI36
NG_023270.1:g.2897_2907del
NG_042828.1:g.7707_7717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-22_600-12del MANE Select	ENSP00000231749.3:n.600-22_600-12del
ENST00000231749.7:c.600-22_600-12del	ENSP00000231749.3:n.600-22_600-12del
ENST00000360165.7:c.599+78_599+88del	ENSP00000353289.3:n.599+78_599+88del
ENST00000442887.1:c.471-22_471-12del	ENSP00000393687.1:n.471-22_471-12del
ENST00000443080.5:c.*352-22_*352-12del	ENSP00000415661.1:n.*352-22_*352-12del
ENST00000475688.1:n.129_139del
NM_001308379.1:c.599+78_599+88del	NP_001295308.1:n.599+78_599+88del
NM_015896.2:c.600-22_600-12del	NP_056980.2:n.600-22_600-12del
NM_015896.3:c.600-22_600-12del	NP_056980.2:n.600-22_600-12del
XM_005265216.2:c.363-22_363-12del	XP_005265273.1:n.363-22_363-12del
XM_005265216.3:c.363-22_363-12del	XP_005265273.1:n.363-22_363-12del
NM_015896.4:c.600-22_600-12del MANE Select	NP_056980.2:n.600-22_600-12del
NM_001308379.2:c.599+78_599+88del	NP_001295308.1:n.599+78_599+88del