Canonical Allele Identifier: CA352946025

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382950T>G (hg19) ; chr3:g.50345519T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345519T>G , CM000665.2:g.50345519T>G	GRCh38
NC_000003.11:g.50382950T>G , CM000665.1:g.50382950T>G	GRCh37
NC_000003.10:g.50357954T>G	NCBI36
NG_023270.1:g.418A>C
NG_042828.1:g.5228A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.61A>C MANE Select	ENSP00000231749.3:p.Ser21Arg
ENST00000231749.7:c.61A>C	ENSP00000231749.3:p.Ser21Arg
ENST00000360165.7:c.61A>C	ENSP00000353289.3:p.Ser21Arg
ENST00000431869.1:c.61A>C	ENSP00000391545.1:p.Ser21Arg
ENST00000442887.1:c.-38+16A>C	ENSP00000393687.1:n.-38+16A>C
ENST00000443080.5:c.61A>C	ENSP00000415661.1:p.Ser21Arg
ENST00000468182.1:n.163A>C
NM_001308379.1:c.61A>C	NP_001295308.1:p.Ser21Arg
NM_015896.2:c.61A>C	NP_056980.2:p.Ser21Arg
NM_015896.3:c.61A>C	NP_056980.2:p.Ser21Arg
XM_005265216.2:c.-68A>C	XP_005265273.1:n.-68A>C
XM_005265216.3:c.-68A>C	XP_005265273.1:n.-68A>C
NM_015896.4:c.61A>C MANE Select	NP_056980.2:p.Ser21Arg
NM_001308379.2:c.61A>C	NP_001295308.1:p.Ser21Arg