Canonical Allele Identifier: CA2665848450

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345657-A-AAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345657_50345658insAATG , CM000665.2:g.50345657_50345658insAATG	GRCh38
NC_000003.11:g.50383088_50383089insAATG , CM000665.1:g.50383088_50383089insAATG	GRCh37
NC_000003.10:g.50358092_50358093insAATG	NCBI36
NG_023270.1:g.279_280insCATT
NG_042828.1:g.5089_5090insCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-79_-78insCATT MANE Select	ENSP00000231749.3:n.-79_-78insCATT
ENST00000231749.7:c.-79_-78insCATT	ENSP00000231749.3:n.-79_-78insCATT
ENST00000360165.7:c.-79_-78insCATT	ENSP00000353289.3:n.-79_-78insCATT
ENST00000431869.1:c.-79_-78insCATT	ENSP00000391545.1:n.-79_-78insCATT
ENST00000442887.1:c.-161_-160insCATT	ENSP00000393687.1:n.-161_-160insCATT
ENST00000443080.5:c.-79_-78insCATT	ENSP00000415661.1:n.-79_-78insCATT
ENST00000468182.1:n.24_25insCATT
NM_001308379.1:c.-79_-78insCATT	NP_001295308.1:n.-79_-78insCATT
NM_015896.2:c.-79_-78insCATT	NP_056980.2:n.-79_-78insCATT
NM_015896.3:c.-79_-78insCATT	NP_056980.2:n.-79_-78insCATT
XM_005265216.2:c.-207_-206insCATT	XP_005265273.1:n.-207_-206insCATT
XM_005265216.3:c.-207_-206insCATT	XP_005265273.1:n.-207_-206insCATT
NM_015896.4:c.-79_-78insCATT MANE Select	NP_056980.2:n.-79_-78insCATT
NM_001308379.2:c.-79_-78insCATT	NP_001295308.1:n.-79_-78insCATT