Canonical Allele Identifier: CA2665853617

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50342792-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342792G>T , CM000665.2:g.50342792G>T	GRCh38
NC_000003.11:g.50380223G>T , CM000665.1:g.50380223G>T	GRCh37
NC_000003.10:g.50355227G>T	NCBI36
NG_023270.1:g.3145C>A
NG_042828.1:g.7955C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+126C>A MANE Select	ENSP00000231749.3:n.700+126C>A
ENST00000231749.7:c.700+126C>A	ENSP00000231749.3:n.700+126C>A
ENST00000360165.7:c.600-137C>A	ENSP00000353289.3:n.600-137C>A
ENST00000442887.1:c.571+126C>A	ENSP00000393687.1:n.571+126C>A
ENST00000443080.5:c.*452+126C>A	ENSP00000415661.1:n.*452+126C>A
ENST00000475688.1:n.377C>A
NM_001308379.1:c.600-137C>A	NP_001295308.1:n.600-137C>A
NM_015896.2:c.700+126C>A	NP_056980.2:n.700+126C>A
NM_015896.3:c.700+126C>A	NP_056980.2:n.700+126C>A
XM_005265216.2:c.463+126C>A	XP_005265273.1:n.463+126C>A
XM_005265216.3:c.463+126C>A	XP_005265273.1:n.463+126C>A
NM_015896.4:c.700+126C>A MANE Select	NP_056980.2:n.700+126C>A
NM_001308379.2:c.600-137C>A	NP_001295308.1:n.600-137C>A