Canonical Allele Identifier: CA352942198

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380599A>C (hg19) ; chr3:g.50343168A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.549T>G MANE Select	ENSP00000231749.3:p.Ile183Met
ENST00000231749.7:c.549T>G	ENSP00000231749.3:p.Ile183Met
ENST00000360165.7:c.549T>G	ENSP00000353289.3:p.Ile183Met
ENST00000442887.1:c.420T>G	ENSP00000393687.1:p.Ile140Met
ENST00000443080.5:c.*301T>G	ENSP00000415661.1:n.*301T>G
ENST00000475688.1:n.1T>G
NM_001308379.1:c.549T>G	NP_001295308.1:p.Ile183Met
NM_015896.2:c.549T>G	NP_056980.2:p.Ile183Met
NM_015896.3:c.549T>G	NP_056980.2:p.Ile183Met
XM_005265216.2:c.312T>G	XP_005265273.1:p.Ile104Met
XM_005265216.3:c.312T>G	XP_005265273.1:p.Ile104Met
NM_015896.4:c.549T>G MANE Select	NP_056980.2:p.Ile183Met
NM_001308379.2:c.549T>G	NP_001295308.1:p.Ile183Met