Canonical Allele Identifier: CA352940495

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342561G>A , CM000665.2:g.50342561G>A	GRCh38
NC_000003.11:g.50379992G>A , CM000665.1:g.50379992G>A	GRCh37
NC_000003.10:g.50354996G>A	NCBI36
NG_023270.1:g.3376C>T
NG_042828.1:g.8186C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015896.4:c.709C>T MANE Select	NP_056980.2:p.Gln237Ter
ENST00000231749.8:c.709C>T MANE Select	ENSP00000231749.3:p.Gln237Ter
NM_001308379.1:c.694C>T	NP_001295308.1:p.Gln232Ter
NM_001308379.2:c.694C>T	NP_001295308.1:p.Gln232Ter
NM_015896.2:c.709C>T	NP_056980.2:p.Gln237Ter
NM_015896.3:c.709C>T	NP_056980.2:p.Gln237Ter
ENST00000231749.7:c.709C>T	ENSP00000231749.3:p.Gln237Ter
ENST00000360165.7:c.694C>T	ENSP00000353289.3:p.Gln232Ter
ENST00000442887.1:c.580C>T	ENSP00000393687.1:p.Gln194Ter
ENST00000443080.5:c.*461C>T	ENSP00000415661.1:n.*461C>T
ENST00000475688.1:n.608C>T
XM_005265216.2:c.472C>T	XP_005265273.1:p.Gln158Ter
XM_005265216.3:c.472C>T	XP_005265273.1:p.Gln158Ter