Canonical Allele Identifier: CA352945518

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382587G>A (hg19) ; chr3:g.50345156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345156G>A , CM000665.2:g.50345156G>A	GRCh38
NC_000003.11:g.50382587G>A , CM000665.1:g.50382587G>A	GRCh37
NC_000003.10:g.50357591G>A	NCBI36
NG_023270.1:g.781C>T
NG_042828.1:g.5591C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.169C>T MANE Select	ENSP00000231749.3:p.Pro57Ser
ENST00000231749.7:c.169C>T	ENSP00000231749.3:p.Pro57Ser
ENST00000360165.7:c.169C>T	ENSP00000353289.3:p.Pro57Ser
ENST00000431869.1:c.*59C>T	ENSP00000391545.1:n.*59C>T
ENST00000442887.1:c.40C>T	ENSP00000393687.1:p.Pro14Ser
ENST00000443080.5:c.*59C>T	ENSP00000415661.1:n.*59C>T
ENST00000468182.1:n.271C>T
NM_001308379.1:c.169C>T	NP_001295308.1:p.Pro57Ser
NM_015896.2:c.169C>T	NP_056980.2:p.Pro57Ser
NM_015896.3:c.169C>T	NP_056980.2:p.Pro57Ser
XM_005265216.2:c.-37+332C>T	XP_005265273.1:n.-37+332C>T
XM_005265216.3:c.-37+332C>T	XP_005265273.1:n.-37+332C>T
NM_015896.4:c.169C>T MANE Select	NP_056980.2:p.Pro57Ser
NM_001308379.2:c.169C>T	NP_001295308.1:p.Pro57Ser