Canonical Allele Identifier: CA2756211677

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342854_50342855dup , CM000665.2:g.50342854_50342855dup	GRCh38
NC_000003.11:g.50380285_50380286dup , CM000665.1:g.50380285_50380286dup	GRCh37
NC_000003.10:g.50355289_50355290dup	NCBI36
NG_023270.1:g.3086_3087dup
NG_042828.1:g.7896_7897dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+67_700+68dup MANE Select	ENSP00000231749.3:n.700+67_700+68dup
ENST00000231749.7:c.700+67_700+68dup	ENSP00000231749.3:n.700+67_700+68dup
ENST00000360165.7:c.600-196_600-195dup	ENSP00000353289.3:n.600-196_600-195dup
ENST00000442887.1:c.571+67_571+68dup	ENSP00000393687.1:n.571+67_571+68dup
ENST00000443080.5:c.*452+67_*452+68dup	ENSP00000415661.1:n.*452+67_*452+68dup
ENST00000475688.1:n.318_319dup
NM_001308379.1:c.600-196_600-195dup	NP_001295308.1:n.600-196_600-195dup
NM_015896.2:c.700+67_700+68dup	NP_056980.2:n.700+67_700+68dup
NM_015896.3:c.700+67_700+68dup	NP_056980.2:n.700+67_700+68dup
XM_005265216.2:c.463+67_463+68dup	XP_005265273.1:n.463+67_463+68dup
XM_005265216.3:c.463+67_463+68dup	XP_005265273.1:n.463+67_463+68dup
NM_015896.4:c.700+67_700+68dup MANE Select	NP_056980.2:n.700+67_700+68dup
NM_001308379.2:c.600-196_600-195dup	NP_001295308.1:n.600-196_600-195dup