Canonical Allele Identifier: CA1363902859
Gene: ZMYND10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50342717G= , CM000665.2:g.50342717G= GRCh38
NC_000003.11:g.50380148G= , CM000665.1:g.50380148G= GRCh37
NC_000003.10:g.50355152G= NCBI36
NG_023270.1:g.3220C=
NG_042828.1:g.8030C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231749.8:c.701-148C= MANE Select ENSP00000231749.3:n.701-148C=
ENST00000231749.7:c.701-148C= ENSP00000231749.3:n.701-148C=
ENST00000360165.7:c.600-62C= ENSP00000353289.3:n.600-62C=
ENST00000442887.1:c.572-148C= ENSP00000393687.1:n.572-148C=
ENST00000443080.5:c.*453-148C= ENSP00000415661.1:n.*453-148C=
ENST00000475688.1:n.452C=
NM_001308379.1:c.600-62C= NP_001295308.1:n.600-62C=
NM_015896.2:c.701-148C= NP_056980.2:n.701-148C=
NM_015896.3:c.701-148C= NP_056980.2:n.701-148C=
XM_005265216.2:c.464-148C= XP_005265273.1:n.464-148C=
XM_005265216.3:c.464-148C= XP_005265273.1:n.464-148C=
NM_015896.4:c.701-148C= MANE Select NP_056980.2:n.701-148C=
NM_001308379.2:c.600-62C= NP_001295308.1:n.600-62C=