Canonical Allele Identifier: CA352945648

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50382617T>G (hg19) ; chr3:g.50345186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345186T>G , CM000665.2:g.50345186T>G	GRCh38
NC_000003.11:g.50382617T>G , CM000665.1:g.50382617T>G	GRCh37
NC_000003.10:g.50357621T>G	NCBI36
NG_023270.1:g.751A>C
NG_042828.1:g.5561A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.139A>C MANE Select	ENSP00000231749.3:p.Ile47Leu
ENST00000231749.7:c.139A>C	ENSP00000231749.3:p.Ile47Leu
ENST00000360165.7:c.139A>C	ENSP00000353289.3:p.Ile47Leu
ENST00000431869.1:c.*29A>C	ENSP00000391545.1:n.*29A>C
ENST00000442887.1:c.10A>C	ENSP00000393687.1:p.Ile4Leu
ENST00000443080.5:c.*29A>C	ENSP00000415661.1:n.*29A>C
ENST00000468182.1:n.241A>C
NM_001308379.1:c.139A>C	NP_001295308.1:p.Ile47Leu
NM_015896.2:c.139A>C	NP_056980.2:p.Ile47Leu
NM_015896.3:c.139A>C	NP_056980.2:p.Ile47Leu
XM_005265216.2:c.-37+302A>C	XP_005265273.1:n.-37+302A>C
XM_005265216.3:c.-37+302A>C	XP_005265273.1:n.-37+302A>C
NM_015896.4:c.139A>C MANE Select	NP_056980.2:p.Ile47Leu
NM_001308379.2:c.139A>C	NP_001295308.1:p.Ile47Leu