Canonical Allele Identifier: CA2665848519

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50345700-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50345700G>T , CM000665.2:g.50345700G>T	GRCh38
NC_000003.11:g.50383131G>T , CM000665.1:g.50383131G>T	GRCh37
NC_000003.10:g.50358135G>T	NCBI36
NG_023270.1:g.237C>A
NG_042828.1:g.5047C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.-121C>A MANE Select	ENSP00000231749.3:n.-121C>A
ENST00000231749.7:c.-121C>A	ENSP00000231749.3:n.-121C>A
ENST00000360165.7:c.-121C>A	ENSP00000353289.3:n.-121C>A
ENST00000431869.1:c.-121C>A	ENSP00000391545.1:n.-121C>A
ENST00000442887.1:c.-203C>A	ENSP00000393687.1:n.-203C>A
NM_001308379.1:c.-121C>A	NP_001295308.1:n.-121C>A
NM_015896.2:c.-121C>A	NP_056980.2:n.-121C>A
NM_015896.3:c.-121C>A	NP_056980.2:n.-121C>A
XM_005265216.2:c.-249C>A	XP_005265273.1:n.-249C>A
NM_015896.4:c.-121C>A MANE Select	NP_056980.2:n.-121C>A
NM_001308379.2:c.-121C>A	NP_001295308.1:n.-121C>A