Canonical Allele Identifier: CA1363902897
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50342796C= , CM000665.2:g.50342796C= GRCh38
NC_000003.11:g.50380227C= , CM000665.1:g.50380227C= GRCh37
NC_000003.10:g.50355231C= NCBI36
NG_023270.1:g.3141G=
NG_042828.1:g.7951G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.700+122G= MANE Select ENSP00000231749.3:n.700+122G=
ENST00000231749.7:c.700+122G= ENSP00000231749.3:n.700+122G=
ENST00000360165.7:c.600-141G= ENSP00000353289.3:n.600-141G=
ENST00000442887.1:c.571+122G= ENSP00000393687.1:n.571+122G=
ENST00000443080.5:c.*452+122G= ENSP00000415661.1:n.*452+122G=
ENST00000475688.1:n.373G=
NM_001308379.1:c.600-141G= NP_001295308.1:n.600-141G=
NM_015896.2:c.700+122G= NP_056980.2:n.700+122G=
NM_015896.3:c.700+122G= NP_056980.2:n.700+122G=
XM_005265216.2:c.463+122G= XP_005265273.1:n.463+122G=
XM_005265216.3:c.463+122G= XP_005265273.1:n.463+122G=
NM_015896.4:c.700+122G= MANE Select NP_056980.2:n.700+122G=
NM_001308379.2:c.600-141G= NP_001295308.1:n.600-141G=