Canonical Allele Identifier: CA352942178

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380592T>A (hg19) ; chr3:g.50343161T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343161T>A , CM000665.2:g.50343161T>A	GRCh38
NC_000003.11:g.50380592T>A , CM000665.1:g.50380592T>A	GRCh37
NC_000003.10:g.50355596T>A	NCBI36
NG_023270.1:g.2776A>T
NG_042828.1:g.7586A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.556A>T MANE Select	ENSP00000231749.3:p.Lys186Ter
ENST00000231749.7:c.556A>T	ENSP00000231749.3:p.Lys186Ter
ENST00000360165.7:c.556A>T	ENSP00000353289.3:p.Lys186Ter
ENST00000442887.1:c.427A>T	ENSP00000393687.1:p.Lys143Ter
ENST00000443080.5:c.*308A>T	ENSP00000415661.1:n.*308A>T
ENST00000475688.1:n.8A>T
NM_001308379.1:c.556A>T	NP_001295308.1:p.Lys186Ter
NM_015896.2:c.556A>T	NP_056980.2:p.Lys186Ter
NM_015896.3:c.556A>T	NP_056980.2:p.Lys186Ter
XM_005265216.2:c.319A>T	XP_005265273.1:p.Lys107Ter
XM_005265216.3:c.319A>T	XP_005265273.1:p.Lys107Ter
NM_015896.4:c.556A>T MANE Select	NP_056980.2:p.Lys186Ter
NM_001308379.2:c.556A>T	NP_001295308.1:p.Lys186Ter