Canonical Allele Identifier: CA2417328
Gene: ZMYND10 HGNC NCBI

Linked Data

dbSNP Id: rs199745411
gnomAD v2: 3-50382943-G-A
gnomAD v3: 3-50345512-G-A
gnomAD v4: 3-50345512-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50345512G>A , CM000665.2:g.50345512G>A GRCh38
NC_000003.11:g.50382943G>A , CM000665.1:g.50382943G>A GRCh37
NC_000003.10:g.50357947G>A NCBI36
NG_023270.1:g.425C>T
NG_042828.1:g.5235C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.68C>T MANE Select ENSP00000231749.3:p.Pro23Leu
ENST00000231749.7:c.68C>T ENSP00000231749.3:p.Pro23Leu
ENST00000360165.7:c.68C>T ENSP00000353289.3:p.Pro23Leu
ENST00000431869.1:c.68C>T ENSP00000391545.1:p.Pro23Leu
ENST00000442887.1:c.-38+23C>T ENSP00000393687.1:n.-38+23C>T
ENST00000443080.5:c.68C>T ENSP00000415661.1:p.Pro23Leu
ENST00000468182.1:n.170C>T
NM_001308379.1:c.68C>T NP_001295308.1:p.Pro23Leu
NM_015896.2:c.68C>T NP_056980.2:p.Pro23Leu
NM_015896.3:c.68C>T NP_056980.2:p.Pro23Leu
XM_005265216.2:c.-61C>T XP_005265273.1:n.-61C>T
XM_005265216.3:c.-61C>T XP_005265273.1:n.-61C>T
NM_015896.4:c.68C>T MANE Select NP_056980.2:p.Pro23Leu
NM_001308379.2:c.68C>T NP_001295308.1:p.Pro23Leu