Canonical Allele Identifier: CA352942195

Gene: ZMYND10

Linked Data

• gnomAD v4: 3-50343167-C-A
• MyVariant Identifiers: chr3:g.50380598C>A (hg19) ; chr3:g.50343167C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50343167C>A , CM000665.2:g.50343167C>A	GRCh38
NC_000003.11:g.50380598C>A , CM000665.1:g.50380598C>A	GRCh37
NC_000003.10:g.50355602C>A	NCBI36
NG_023270.1:g.2770G>T
NG_042828.1:g.7580G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.550G>T MANE Select	ENSP00000231749.3:p.Ala184Ser
ENST00000231749.7:c.550G>T	ENSP00000231749.3:p.Ala184Ser
ENST00000360165.7:c.550G>T	ENSP00000353289.3:p.Ala184Ser
ENST00000442887.1:c.421G>T	ENSP00000393687.1:p.Ala141Ser
ENST00000443080.5:c.*302G>T	ENSP00000415661.1:n.*302G>T
ENST00000475688.1:n.2G>T
NM_001308379.1:c.550G>T	NP_001295308.1:p.Ala184Ser
NM_015896.2:c.550G>T	NP_056980.2:p.Ala184Ser
NM_015896.3:c.550G>T	NP_056980.2:p.Ala184Ser
XM_005265216.2:c.313G>T	XP_005265273.1:p.Ala105Ser
XM_005265216.3:c.313G>T	XP_005265273.1:p.Ala105Ser
NM_015896.4:c.550G>T MANE Select	NP_056980.2:p.Ala184Ser
NM_001308379.2:c.550G>T	NP_001295308.1:p.Ala184Ser