Canonical Allele Identifier: CA352942090

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380566G>C (hg19) ; chr3:g.50343135G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343135G>C , CM000665.2:g.50343135G>C	GRCh38
NC_000003.11:g.50380566G>C , CM000665.1:g.50380566G>C	GRCh37
NC_000003.10:g.50355570G>C	NCBI36
NG_023270.1:g.2802C>G
NG_042828.1:g.7612C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.582C>G MANE Select	ENSP00000231749.3:p.Ile194Met
ENST00000231749.7:c.582C>G	ENSP00000231749.3:p.Ile194Met
ENST00000360165.7:c.582C>G	ENSP00000353289.3:p.Ile194Met
ENST00000442887.1:c.453C>G	ENSP00000393687.1:p.Ile151Met
ENST00000443080.5:c.*334C>G	ENSP00000415661.1:n.*334C>G
ENST00000475688.1:n.34C>G
NM_001308379.1:c.582C>G	NP_001295308.1:p.Ile194Met
NM_015896.2:c.582C>G	NP_056980.2:p.Ile194Met
NM_015896.3:c.582C>G	NP_056980.2:p.Ile194Met
XM_005265216.2:c.345C>G	XP_005265273.1:p.Ile115Met
XM_005265216.3:c.345C>G	XP_005265273.1:p.Ile115Met
NM_015896.4:c.582C>G MANE Select	NP_056980.2:p.Ile194Met
NM_001308379.2:c.582C>G	NP_001295308.1:p.Ile194Met