Canonical Allele Identifier: CA352945719
Gene: ZMYND10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345203T>G , CM000665.2:g.50345203T>G GRCh38
NC_000003.11:g.50382634T>G , CM000665.1:g.50382634T>G GRCh37
NC_000003.10:g.50357638T>G NCBI36
NG_023270.1:g.734A>C
NG_042828.1:g.5544A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.122A>C MANE Select ENSP00000231749.3:p.Lys41Thr
ENST00000231749.7:c.122A>C ENSP00000231749.3:p.Lys41Thr
ENST00000360165.7:c.122A>C ENSP00000353289.3:p.Lys41Thr
ENST00000431869.1:c.*12A>C ENSP00000391545.1:n.*12A>C
ENST00000442887.1:c.-8A>C ENSP00000393687.1:n.-8A>C
ENST00000443080.5:c.*12A>C ENSP00000415661.1:n.*12A>C
ENST00000468182.1:n.224A>C
NM_001308379.1:c.122A>C NP_001295308.1:p.Lys41Thr
NM_015896.2:c.122A>C NP_056980.2:p.Lys41Thr
NM_015896.3:c.122A>C NP_056980.2:p.Lys41Thr
XM_005265216.2:c.-37+285A>C XP_005265273.1:n.-37+285A>C
XM_005265216.3:c.-37+285A>C XP_005265273.1:n.-37+285A>C
NM_015896.4:c.122A>C MANE Select NP_056980.2:p.Lys41Thr
NM_001308379.2:c.122A>C NP_001295308.1:p.Lys41Thr