Canonical Allele Identifier: CA1363902856

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1703425214
• gnomAD v4: 3-50342709-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342713del , CM000665.2:g.50342713del	GRCh38
NC_000003.11:g.50380144del , CM000665.1:g.50380144del	GRCh37
NC_000003.10:g.50355148del	NCBI36
NG_023270.1:g.3227del
NG_042828.1:g.8037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-141del MANE Select	ENSP00000231749.3:n.701-141del
ENST00000231749.7:c.701-141del	ENSP00000231749.3:n.701-141del
ENST00000360165.7:c.600-55del	ENSP00000353289.3:n.600-55del
ENST00000442887.1:c.572-141del	ENSP00000393687.1:n.572-141del
ENST00000443080.5:c.*453-141del	ENSP00000415661.1:n.*453-141del
ENST00000475688.1:n.459del
NM_001308379.1:c.600-55del	NP_001295308.1:n.600-55del
NM_015896.2:c.701-141del	NP_056980.2:n.701-141del
NM_015896.3:c.701-141del	NP_056980.2:n.701-141del
XM_005265216.2:c.464-141del	XP_005265273.1:n.464-141del
XM_005265216.3:c.464-141del	XP_005265273.1:n.464-141del
NM_015896.4:c.701-141del MANE Select	NP_056980.2:n.701-141del
NM_001308379.2:c.600-55del	NP_001295308.1:n.600-55del