Canonical Allele Identifier: CA907889745

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1204391515
• gnomAD v3: 3-50342907-GA-G
• gnomAD v4: 3-50342907-GA-G
• MyVariant Identifiers: chr3:g.50380339del (hg19) ; chr3:g.50342908del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342908del , CM000665.2:g.50342908del	GRCh38
NC_000003.11:g.50380339del , CM000665.1:g.50380339del	GRCh37
NC_000003.10:g.50355343del	NCBI36
NG_023270.1:g.3029del
NG_042828.1:g.7839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+10del MANE Select	ENSP00000231749.3:n.700+10del
ENST00000231749.7:c.700+10del	ENSP00000231749.3:n.700+10del
ENST00000360165.7:c.599+210del	ENSP00000353289.3:n.599+210del
ENST00000442887.1:c.571+10del	ENSP00000393687.1:n.571+10del
ENST00000443080.5:c.*452+10del	ENSP00000415661.1:n.*452+10del
ENST00000475688.1:n.261del
NM_001308379.1:c.599+210del	NP_001295308.1:n.599+210del
NM_015896.2:c.700+10del	NP_056980.2:n.700+10del
NM_015896.3:c.700+10del	NP_056980.2:n.700+10del
XM_005265216.2:c.463+10del	XP_005265273.1:n.463+10del
XM_005265216.3:c.463+10del	XP_005265273.1:n.463+10del
NM_015896.4:c.700+10del MANE Select	NP_056980.2:n.700+10del
NM_001308379.2:c.599+210del	NP_001295308.1:n.599+210del