Canonical Allele Identifier: CA2665853647

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50342826-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342826G>T , CM000665.2:g.50342826G>T	GRCh38
NC_000003.11:g.50380257G>T , CM000665.1:g.50380257G>T	GRCh37
NC_000003.10:g.50355261G>T	NCBI36
NG_023270.1:g.3111C>A
NG_042828.1:g.7921C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+92C>A MANE Select	ENSP00000231749.3:n.700+92C>A
ENST00000231749.7:c.700+92C>A	ENSP00000231749.3:n.700+92C>A
ENST00000360165.7:c.600-171C>A	ENSP00000353289.3:n.600-171C>A
ENST00000442887.1:c.571+92C>A	ENSP00000393687.1:n.571+92C>A
ENST00000443080.5:c.*452+92C>A	ENSP00000415661.1:n.*452+92C>A
ENST00000475688.1:n.343C>A
NM_001308379.1:c.600-171C>A	NP_001295308.1:n.600-171C>A
NM_015896.2:c.700+92C>A	NP_056980.2:n.700+92C>A
NM_015896.3:c.700+92C>A	NP_056980.2:n.700+92C>A
XM_005265216.2:c.463+92C>A	XP_005265273.1:n.463+92C>A
XM_005265216.3:c.463+92C>A	XP_005265273.1:n.463+92C>A
NM_015896.4:c.700+92C>A MANE Select	NP_056980.2:n.700+92C>A
NM_001308379.2:c.600-171C>A	NP_001295308.1:n.600-171C>A