Canonical Allele Identifier: CA907891954

Gene: ZMYND10

Linked Data

• dbSNP Id: rs1227891969
• gnomAD v3: 3-50345651-A-AC
• gnomAD v4: 3-50345651-A-AC
• MyVariant Identifiers: chr3:g.50383082_50383083insC (hg19) ; chr3:g.50345651_50345652insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345655dup , CM000665.2:g.50345655dup	GRCh38
NC_000003.11:g.50383086dup , CM000665.1:g.50383086dup	GRCh37
NC_000003.10:g.50358090dup	NCBI36
NG_023270.1:g.285dup
NG_042828.1:g.5095dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-73dup MANE Select	ENSP00000231749.3:n.-73dup
ENST00000231749.7:c.-73dup	ENSP00000231749.3:n.-73dup
ENST00000360165.7:c.-73dup	ENSP00000353289.3:n.-73dup
ENST00000431869.1:c.-73dup	ENSP00000391545.1:n.-73dup
ENST00000442887.1:c.-155dup	ENSP00000393687.1:n.-155dup
ENST00000443080.5:c.-73dup	ENSP00000415661.1:n.-73dup
ENST00000468182.1:n.30dup
NM_001308379.1:c.-73dup	NP_001295308.1:n.-73dup
NM_015896.2:c.-73dup	NP_056980.2:n.-73dup
NM_015896.3:c.-73dup	NP_056980.2:n.-73dup
XM_005265216.2:c.-201dup	XP_005265273.1:n.-201dup
XM_005265216.3:c.-201dup	XP_005265273.1:n.-201dup
NM_015896.4:c.-73dup MANE Select	NP_056980.2:n.-73dup
NM_001308379.2:c.-73dup	NP_001295308.1:n.-73dup