Canonical Allele Identifier: CA1363908784

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345492_50345493delinsCG , CM000665.2:g.50345492_50345493delinsCG	GRCh38
NC_000003.11:g.50382923_50382924delinsCG , CM000665.1:g.50382923_50382924delinsCG	GRCh37
NC_000003.10:g.50357927_50357928delinsCG	NCBI36
NG_023270.1:g.444_445delinsCG
NG_042828.1:g.5254_5255delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.87_88delinsCG MANE Select	ENSP00000231749.3:p.Ser29=
ENST00000231749.7:c.87_88delinsCG	ENSP00000231749.3:p.Ser29=
ENST00000360165.7:c.87_88delinsCG	ENSP00000353289.3:p.Ser29=
ENST00000431869.1:c.87_88delinsCG	ENSP00000391545.1:p.Ser29=
ENST00000442887.1:c.-38+42_-38+43delinsCG	ENSP00000393687.1:n.-38+42_-38+43delinsCG
ENST00000443080.5:c.87_88delinsCG	ENSP00000415661.1:p.Ser29=
ENST00000468182.1:n.189_190delinsCG
NM_001308379.1:c.87_88delinsCG	NP_001295308.1:p.Ser29=
NM_015896.2:c.87_88delinsCG	NP_056980.2:p.Ser29=
NM_015896.3:c.87_88delinsCG	NP_056980.2:p.Ser29=
XM_005265216.2:c.-42_-41delinsCG	XP_005265273.1:n.-42_-41delinsCG
XM_005265216.3:c.-42_-41delinsCG	XP_005265273.1:n.-42_-41delinsCG
NM_015896.4:c.87_88delinsCG MANE Select	NP_056980.2:p.Ser29=
NM_001308379.2:c.87_88delinsCG	NP_001295308.1:p.Ser29=