Canonical Allele Identifier: CA352942185

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380594A>T (hg19) ; chr3:g.50343163A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343163A>T , CM000665.2:g.50343163A>T	GRCh38
NC_000003.11:g.50380594A>T , CM000665.1:g.50380594A>T	GRCh37
NC_000003.10:g.50355598A>T	NCBI36
NG_023270.1:g.2774T>A
NG_042828.1:g.7584T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.554T>A MANE Select	ENSP00000231749.3:p.Leu185Gln
ENST00000231749.7:c.554T>A	ENSP00000231749.3:p.Leu185Gln
ENST00000360165.7:c.554T>A	ENSP00000353289.3:p.Leu185Gln
ENST00000442887.1:c.425T>A	ENSP00000393687.1:p.Leu142Gln
ENST00000443080.5:c.*306T>A	ENSP00000415661.1:n.*306T>A
ENST00000475688.1:n.6T>A
NM_001308379.1:c.554T>A	NP_001295308.1:p.Leu185Gln
NM_015896.2:c.554T>A	NP_056980.2:p.Leu185Gln
NM_015896.3:c.554T>A	NP_056980.2:p.Leu185Gln
XM_005265216.2:c.317T>A	XP_005265273.1:p.Leu106Gln
XM_005265216.3:c.317T>A	XP_005265273.1:p.Leu106Gln
NM_015896.4:c.554T>A MANE Select	NP_056980.2:p.Leu185Gln
NM_001308379.2:c.554T>A	NP_001295308.1:p.Leu185Gln