Canonical Allele Identifier: CA2665853521

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50342714-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342714A>C , CM000665.2:g.50342714A>C	GRCh38
NC_000003.11:g.50380145A>C , CM000665.1:g.50380145A>C	GRCh37
NC_000003.10:g.50355149A>C	NCBI36
NG_023270.1:g.3223T>G
NG_042828.1:g.8033T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.701-145T>G MANE Select	ENSP00000231749.3:n.701-145T>G
ENST00000231749.7:c.701-145T>G	ENSP00000231749.3:n.701-145T>G
ENST00000360165.7:c.600-59T>G	ENSP00000353289.3:n.600-59T>G
ENST00000442887.1:c.572-145T>G	ENSP00000393687.1:n.572-145T>G
ENST00000443080.5:c.*453-145T>G	ENSP00000415661.1:n.*453-145T>G
ENST00000475688.1:n.455T>G
NM_001308379.1:c.600-59T>G	NP_001295308.1:n.600-59T>G
NM_015896.2:c.701-145T>G	NP_056980.2:n.701-145T>G
NM_015896.3:c.701-145T>G	NP_056980.2:n.701-145T>G
XM_005265216.2:c.464-145T>G	XP_005265273.1:n.464-145T>G
XM_005265216.3:c.464-145T>G	XP_005265273.1:n.464-145T>G
NM_015896.4:c.701-145T>G MANE Select	NP_056980.2:n.701-145T>G
NM_001308379.2:c.600-59T>G	NP_001295308.1:n.600-59T>G