Canonical Allele Identifier: CA2756211934

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345463_50345464insG , CM000665.2:g.50345463_50345464insG	GRCh38
NC_000003.11:g.50382894_50382895insG , CM000665.1:g.50382894_50382895insG	GRCh37
NC_000003.10:g.50357898_50357899insG	NCBI36
NG_023270.1:g.473_474insC
NG_042828.1:g.5283_5284insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.92+24_92+25insC MANE Select	ENSP00000231749.3:n.92+24_92+25insC
ENST00000231749.7:c.92+24_92+25insC	ENSP00000231749.3:n.92+24_92+25insC
ENST00000360165.7:c.92+24_92+25insC	ENSP00000353289.3:n.92+24_92+25insC
ENST00000431869.1:c.92+24_92+25insC	ENSP00000391545.1:n.92+24_92+25insC
ENST00000442887.1:c.-38+71_-38+72insC	ENSP00000393687.1:n.-38+71_-38+72insC
ENST00000443080.5:c.92+24_92+25insC	ENSP00000415661.1:n.92+24_92+25insC
ENST00000468182.1:n.194+24_194+25insC
NM_001308379.1:c.92+24_92+25insC	NP_001295308.1:n.92+24_92+25insC
NM_015896.2:c.92+24_92+25insC	NP_056980.2:n.92+24_92+25insC
NM_015896.3:c.92+24_92+25insC	NP_056980.2:n.92+24_92+25insC
XM_005265216.2:c.-37+24_-37+25insC	XP_005265273.1:n.-37+24_-37+25insC
XM_005265216.3:c.-37+24_-37+25insC	XP_005265273.1:n.-37+24_-37+25insC
NM_015896.4:c.92+24_92+25insC MANE Select	NP_056980.2:n.92+24_92+25insC
NM_001308379.2:c.92+24_92+25insC	NP_001295308.1:n.92+24_92+25insC