Canonical Allele Identifier: CA352945588

Gene: ZMYND10

Linked Data

• ClinVar Variation Id: 2990294
• ClinVar RCV Id: RCV003844989
• MyVariant Identifiers: chr3:g.50382604G>A (hg19) ; chr3:g.50345173G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345173G>A , CM000665.2:g.50345173G>A	GRCh38
NC_000003.11:g.50382604G>A , CM000665.1:g.50382604G>A	GRCh37
NC_000003.10:g.50357608G>A	NCBI36
NG_023270.1:g.764C>T
NG_042828.1:g.5574C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.152C>T MANE Select	ENSP00000231749.3:p.Thr51Ile
ENST00000231749.7:c.152C>T	ENSP00000231749.3:p.Thr51Ile
ENST00000360165.7:c.152C>T	ENSP00000353289.3:p.Thr51Ile
ENST00000431869.1:c.*42C>T	ENSP00000391545.1:n.*42C>T
ENST00000442887.1:c.23C>T	ENSP00000393687.1:p.Thr8Ile
ENST00000443080.5:c.*42C>T	ENSP00000415661.1:n.*42C>T
ENST00000468182.1:n.254C>T
NM_001308379.1:c.152C>T	NP_001295308.1:p.Thr51Ile
NM_015896.2:c.152C>T	NP_056980.2:p.Thr51Ile
NM_015896.3:c.152C>T	NP_056980.2:p.Thr51Ile
XM_005265216.2:c.-37+315C>T	XP_005265273.1:n.-37+315C>T
XM_005265216.3:c.-37+315C>T	XP_005265273.1:n.-37+315C>T
NM_015896.4:c.152C>T MANE Select	NP_056980.2:p.Thr51Ile
NM_001308379.2:c.152C>T	NP_001295308.1:p.Thr51Ile