Canonical Allele Identifier: CA1363903273

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343138G= , CM000665.2:g.50343138G=	GRCh38
NC_000003.11:g.50380569G= , CM000665.1:g.50380569G=	GRCh37
NC_000003.10:g.50355573G=	NCBI36
NG_023270.1:g.2799C=
NG_042828.1:g.7609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.579C= MANE Select	ENSP00000231749.3:p.Tyr193=
ENST00000231749.7:c.579C=	ENSP00000231749.3:p.Tyr193=
ENST00000360165.7:c.579C=	ENSP00000353289.3:p.Tyr193=
ENST00000442887.1:c.450C=	ENSP00000393687.1:p.Tyr150=
ENST00000443080.5:c.*331C=	ENSP00000415661.1:n.*331C=
ENST00000475688.1:n.31C=
NM_001308379.1:c.579C=	NP_001295308.1:p.Tyr193=
NM_015896.2:c.579C=	NP_056980.2:p.Tyr193=
NM_015896.3:c.579C=	NP_056980.2:p.Tyr193=
XM_005265216.2:c.342C=	XP_005265273.1:p.Tyr114=
XM_005265216.3:c.342C=	XP_005265273.1:p.Tyr114=
NM_015896.4:c.579C= MANE Select	NP_056980.2:p.Tyr193=
NM_001308379.2:c.579C=	NP_001295308.1:p.Tyr193=