Canonical Allele Identifier: CA2665853550

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50342733-T-TAGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342735_50342739dup , CM000665.2:g.50342735_50342739dup	GRCh38
NC_000003.11:g.50380166_50380170dup , CM000665.1:g.50380166_50380170dup	GRCh37
NC_000003.10:g.50355170_50355174dup	NCBI36
NG_023270.1:g.3199_3203dup
NG_042828.1:g.8009_8013dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-169_701-165dup MANE Select	ENSP00000231749.3:n.701-169_701-165dup
ENST00000231749.7:c.701-169_701-165dup	ENSP00000231749.3:n.701-169_701-165dup
ENST00000360165.7:c.600-83_600-79dup	ENSP00000353289.3:n.600-83_600-79dup
ENST00000442887.1:c.572-169_572-165dup	ENSP00000393687.1:n.572-169_572-165dup
ENST00000443080.5:c.*453-169_*453-165dup	ENSP00000415661.1:n.*453-169_*453-165dup
ENST00000475688.1:n.431_435dup
NM_001308379.1:c.600-83_600-79dup	NP_001295308.1:n.600-83_600-79dup
NM_015896.2:c.701-169_701-165dup	NP_056980.2:n.701-169_701-165dup
NM_015896.3:c.701-169_701-165dup	NP_056980.2:n.701-169_701-165dup
XM_005265216.2:c.464-169_464-165dup	XP_005265273.1:n.464-169_464-165dup
XM_005265216.3:c.464-169_464-165dup	XP_005265273.1:n.464-169_464-165dup
NM_015896.4:c.701-169_701-165dup MANE Select	NP_056980.2:n.701-169_701-165dup
NM_001308379.2:c.600-83_600-79dup	NP_001295308.1:n.600-83_600-79dup