Canonical Allele Identifier: CA1363907700

Gene: ZMYND10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343285_50343286delinsAC , CM000665.2:g.50343285_50343286delinsAC	GRCh38
NC_000003.11:g.50380716_50380717delinsAC , CM000665.1:g.50380716_50380717delinsAC	GRCh37
NC_000003.10:g.50355720_50355721delinsAC	NCBI36
NG_023270.1:g.2651_2652delinsGT
NG_042828.1:g.7461_7462delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.510+21_510+22delinsGT MANE Select	ENSP00000231749.3:n.510+21_510+22delinsGT
ENST00000231749.7:c.510+21_510+22delinsGT	ENSP00000231749.3:n.510+21_510+22delinsGT
ENST00000360165.7:c.510+21_510+22delinsGT	ENSP00000353289.3:n.510+21_510+22delinsGT
ENST00000442887.1:c.381+21_381+22delinsGT	ENSP00000393687.1:n.381+21_381+22delinsGT
ENST00000443080.5:c.*263-80_*263-79delinsGT	ENSP00000415661.1:n.*263-80_*263-79delinsGT
ENST00000478269.5:n.516_517delinsGT
NM_001308379.1:c.510+21_510+22delinsGT	NP_001295308.1:n.510+21_510+22delinsGT
NM_015896.2:c.510+21_510+22delinsGT	NP_056980.2:n.510+21_510+22delinsGT
NM_015896.3:c.510+21_510+22delinsGT	NP_056980.2:n.510+21_510+22delinsGT
XM_005265216.2:c.273+21_273+22delinsGT	XP_005265273.1:n.273+21_273+22delinsGT
XM_005265216.3:c.273+21_273+22delinsGT	XP_005265273.1:n.273+21_273+22delinsGT
NM_015896.4:c.510+21_510+22delinsGT MANE Select	NP_056980.2:n.510+21_510+22delinsGT
NM_001308379.2:c.510+21_510+22delinsGT	NP_001295308.1:n.510+21_510+22delinsGT