Canonical Allele Identifier: CA2832534303

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342906_50342907del , CM000665.2:g.50342906_50342907del	GRCh38
NC_000003.11:g.50380337_50380338del , CM000665.1:g.50380337_50380338del	GRCh37
NC_000003.10:g.50355341_50355342del	NCBI36
NG_023270.1:g.3033_3034del
NG_042828.1:g.7843_7844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+14_700+15del MANE Select	ENSP00000231749.3:n.700+14_700+15del
ENST00000231749.7:c.700+14_700+15del	ENSP00000231749.3:n.700+14_700+15del
ENST00000360165.7:c.599+214_599+215del	ENSP00000353289.3:n.599+214_599+215del
ENST00000442887.1:c.571+14_571+15del	ENSP00000393687.1:n.571+14_571+15del
ENST00000443080.5:c.*452+14_*452+15del	ENSP00000415661.1:n.*452+14_*452+15del
ENST00000475688.1:n.265_266del
NM_001308379.1:c.599+214_599+215del	NP_001295308.1:n.599+214_599+215del
NM_015896.2:c.700+14_700+15del	NP_056980.2:n.700+14_700+15del
NM_015896.3:c.700+14_700+15del	NP_056980.2:n.700+14_700+15del
XM_005265216.2:c.463+14_463+15del	XP_005265273.1:n.463+14_463+15del
XM_005265216.3:c.463+14_463+15del	XP_005265273.1:n.463+14_463+15del
NM_015896.4:c.700+14_700+15del MANE Select	NP_056980.2:n.700+14_700+15del
NM_001308379.2:c.599+214_599+215del	NP_001295308.1:n.599+214_599+215del