Canonical Allele Identifier: CA2756211935

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345466_50345467del , CM000665.2:g.50345466_50345467del	GRCh38
NC_000003.11:g.50382897_50382898del , CM000665.1:g.50382897_50382898del	GRCh37
NC_000003.10:g.50357901_50357902del	NCBI36
NG_023270.1:g.470_471del
NG_042828.1:g.5280_5281del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.92+21_92+22del MANE Select	ENSP00000231749.3:n.92+21_92+22del
ENST00000231749.7:c.92+21_92+22del	ENSP00000231749.3:n.92+21_92+22del
ENST00000360165.7:c.92+21_92+22del	ENSP00000353289.3:n.92+21_92+22del
ENST00000431869.1:c.92+21_92+22del	ENSP00000391545.1:n.92+21_92+22del
ENST00000442887.1:c.-38+68_-38+69del	ENSP00000393687.1:n.-38+68_-38+69del
ENST00000443080.5:c.92+21_92+22del	ENSP00000415661.1:n.92+21_92+22del
ENST00000468182.1:n.194+21_194+22del
NM_001308379.1:c.92+21_92+22del	NP_001295308.1:n.92+21_92+22del
NM_015896.2:c.92+21_92+22del	NP_056980.2:n.92+21_92+22del
NM_015896.3:c.92+21_92+22del	NP_056980.2:n.92+21_92+22del
XM_005265216.2:c.-37+21_-37+22del	XP_005265273.1:n.-37+21_-37+22del
XM_005265216.3:c.-37+21_-37+22del	XP_005265273.1:n.-37+21_-37+22del
NM_015896.4:c.92+21_92+22del MANE Select	NP_056980.2:n.92+21_92+22del
NM_001308379.2:c.92+21_92+22del	NP_001295308.1:n.92+21_92+22del