Canonical Allele Identifier: CA352945758

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382643T>C (hg19) ; chr3:g.50345212T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345212T>C , CM000665.2:g.50345212T>C	GRCh38
NC_000003.11:g.50382643T>C , CM000665.1:g.50382643T>C	GRCh37
NC_000003.10:g.50357647T>C	NCBI36
NG_023270.1:g.725A>G
NG_042828.1:g.5535A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.113A>G MANE Select	ENSP00000231749.3:p.Asn38Ser
ENST00000231749.7:c.113A>G	ENSP00000231749.3:p.Asn38Ser
ENST00000360165.7:c.113A>G	ENSP00000353289.3:p.Asn38Ser
ENST00000431869.1:c.*3A>G	ENSP00000391545.1:n.*3A>G
ENST00000442887.1:c.-17A>G	ENSP00000393687.1:n.-17A>G
ENST00000443080.5:c.*3A>G	ENSP00000415661.1:n.*3A>G
ENST00000468182.1:n.215A>G
NM_001308379.1:c.113A>G	NP_001295308.1:p.Asn38Ser
NM_015896.2:c.113A>G	NP_056980.2:p.Asn38Ser
NM_015896.3:c.113A>G	NP_056980.2:p.Asn38Ser
XM_005265216.2:c.-37+276A>G	XP_005265273.1:n.-37+276A>G
XM_005265216.3:c.-37+276A>G	XP_005265273.1:n.-37+276A>G
NM_015896.4:c.113A>G MANE Select	NP_056980.2:p.Asn38Ser
NM_001308379.2:c.113A>G	NP_001295308.1:p.Asn38Ser