Canonical Allele Identifier: CA352946096

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382971C>T (hg19) ; chr3:g.50345540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345540C>T , CM000665.2:g.50345540C>T	GRCh38
NC_000003.11:g.50382971C>T , CM000665.1:g.50382971C>T	GRCh37
NC_000003.10:g.50357975C>T	NCBI36
NG_023270.1:g.397G>A
NG_042828.1:g.5207G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000231749.8:c.40G>A MANE Select	ENSP00000231749.3:p.Val14Met
ENST00000231749.7:c.40G>A	ENSP00000231749.3:p.Val14Met
ENST00000360165.7:c.40G>A	ENSP00000353289.3:p.Val14Met
ENST00000431869.1:c.40G>A	ENSP00000391545.1:p.Val14Met
ENST00000442887.1:c.-43G>A	ENSP00000393687.1:n.-43G>A
ENST00000443080.5:c.40G>A	ENSP00000415661.1:p.Val14Met
ENST00000468182.1:n.142G>A
NM_001308379.1:c.40G>A	NP_001295308.1:p.Val14Met
NM_015896.2:c.40G>A	NP_056980.2:p.Val14Met
NM_015896.3:c.40G>A	NP_056980.2:p.Val14Met
XM_005265216.2:c.-89G>A	XP_005265273.1:n.-89G>A
XM_005265216.3:c.-89G>A	XP_005265273.1:n.-89G>A
NM_015896.4:c.40G>A MANE Select	NP_056980.2:p.Val14Met
NM_001308379.2:c.40G>A	NP_001295308.1:p.Val14Met