Canonical Allele Identifier: CA433709439

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380599A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343168A>G , CM000665.2:g.50343168A>G	GRCh38
NC_000003.11:g.50380599A>G , CM000665.1:g.50380599A>G	GRCh37
NC_000003.10:g.50355603A>G	NCBI36
NG_023270.1:g.2769T>C
NG_042828.1:g.7579T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.549T>C MANE Select	ENSP00000231749.3:p.Ile183=
ENST00000231749.7:c.549T>C	ENSP00000231749.3:p.Ile183=
ENST00000360165.7:c.549T>C	ENSP00000353289.3:p.Ile183=
ENST00000442887.1:c.420T>C	ENSP00000393687.1:p.Ile140=
ENST00000443080.5:c.*301T>C	ENSP00000415661.1:n.*301T>C
ENST00000475688.1:n.1T>C
NM_001308379.1:c.549T>C	NP_001295308.1:p.Ile183=
NM_015896.2:c.549T>C	NP_056980.2:p.Ile183=
NM_015896.3:c.549T>C	NP_056980.2:p.Ile183=
XM_005265216.2:c.312T>C	XP_005265273.1:p.Ile104=
XM_005265216.3:c.312T>C	XP_005265273.1:p.Ile104=
NM_015896.4:c.549T>C MANE Select	NP_056980.2:p.Ile183=
NM_001308379.2:c.549T>C	NP_001295308.1:p.Ile183=