Canonical Allele Identifier: CA1363903191

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343039_50343042delinsAAGG , CM000665.2:g.50343039_50343042delinsAAGG	GRCh38
NC_000003.11:g.50380470_50380473delinsAAGG , CM000665.1:g.50380470_50380473delinsAAGG	GRCh37
NC_000003.10:g.50355474_50355477delinsAAGG	NCBI36
NG_023270.1:g.2895_2898delinsCCTT
NG_042828.1:g.7705_7708delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.600-24_600-21delinsCCTT MANE Select	ENSP00000231749.3:n.600-24_600-21delinsCCTT
ENST00000231749.7:c.600-24_600-21delinsCCTT	ENSP00000231749.3:n.600-24_600-21delinsCCTT
ENST00000360165.7:c.599+76_599+79delinsCCTT	ENSP00000353289.3:n.599+76_599+79delinsCCTT
ENST00000442887.1:c.471-24_471-21delinsCCTT	ENSP00000393687.1:n.471-24_471-21delinsCCTT
ENST00000443080.5:c.*352-24_*352-21delinsCCTT	ENSP00000415661.1:n.*352-24_*352-21delinsCCTT
ENST00000475688.1:n.127_130delinsCCTT
NM_001308379.1:c.599+76_599+79delinsCCTT	NP_001295308.1:n.599+76_599+79delinsCCTT
NM_015896.2:c.600-24_600-21delinsCCTT	NP_056980.2:n.600-24_600-21delinsCCTT
NM_015896.3:c.600-24_600-21delinsCCTT	NP_056980.2:n.600-24_600-21delinsCCTT
XM_005265216.2:c.363-24_363-21delinsCCTT	XP_005265273.1:n.363-24_363-21delinsCCTT
XM_005265216.3:c.363-24_363-21delinsCCTT	XP_005265273.1:n.363-24_363-21delinsCCTT
NM_015896.4:c.600-24_600-21delinsCCTT MANE Select	NP_056980.2:n.600-24_600-21delinsCCTT
NM_001308379.2:c.599+76_599+79delinsCCTT	NP_001295308.1:n.599+76_599+79delinsCCTT