Canonical Allele Identifier: CA352945969

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2694149
• ClinVar RCV Id: RCV003535071
• gnomAD v4: 3-50345504-C-A
• MyVariant Identifiers: chr3:g.50382935C>A (hg19) ; chr3:g.50345504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345504C>A , CM000665.2:g.50345504C>A	GRCh38
NC_000003.11:g.50382935C>A , CM000665.1:g.50382935C>A	GRCh37
NC_000003.10:g.50357939C>A	NCBI36
NG_023270.1:g.433G>T
NG_042828.1:g.5243G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.76G>T MANE Select	ENSP00000231749.3:p.Glu26Ter
ENST00000231749.7:c.76G>T	ENSP00000231749.3:p.Glu26Ter
ENST00000360165.7:c.76G>T	ENSP00000353289.3:p.Glu26Ter
ENST00000431869.1:c.76G>T	ENSP00000391545.1:p.Glu26Ter
ENST00000442887.1:c.-38+31G>T	ENSP00000393687.1:n.-38+31G>T
ENST00000443080.5:c.76G>T	ENSP00000415661.1:p.Glu26Ter
ENST00000468182.1:n.178G>T
NM_001308379.1:c.76G>T	NP_001295308.1:p.Glu26Ter
NM_015896.2:c.76G>T	NP_056980.2:p.Glu26Ter
NM_015896.3:c.76G>T	NP_056980.2:p.Glu26Ter
XM_005265216.2:c.-53G>T	XP_005265273.1:n.-53G>T
XM_005265216.3:c.-53G>T	XP_005265273.1:n.-53G>T
NM_015896.4:c.76G>T MANE Select	NP_056980.2:p.Glu26Ter
NM_001308379.2:c.76G>T	NP_001295308.1:p.Glu26Ter