Canonical Allele Identifier: CA352941901

Gene: ZMYND10

Linked Data

• MyVariant Identifiers: chr3:g.50380418T>G (hg19) ; chr3:g.50342987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342987T>G , CM000665.2:g.50342987T>G	GRCh38
NC_000003.11:g.50380418T>G , CM000665.1:g.50380418T>G	GRCh37
NC_000003.10:g.50355422T>G	NCBI36
NG_023270.1:g.2950A>C
NG_042828.1:g.7760A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.631A>C MANE Select	ENSP00000231749.3:p.Ser211Arg
ENST00000231749.7:c.631A>C	ENSP00000231749.3:p.Ser211Arg
ENST00000360165.7:c.599+131A>C	ENSP00000353289.3:n.599+131A>C
ENST00000442887.1:c.502A>C	ENSP00000393687.1:p.Ser168Arg
ENST00000443080.5:c.*383A>C	ENSP00000415661.1:n.*383A>C
ENST00000475688.1:n.182A>C
NM_001308379.1:c.599+131A>C	NP_001295308.1:n.599+131A>C
NM_015896.2:c.631A>C	NP_056980.2:p.Ser211Arg
NM_015896.3:c.631A>C	NP_056980.2:p.Ser211Arg
XM_005265216.2:c.394A>C	XP_005265273.1:p.Ser132Arg
XM_005265216.3:c.394A>C	XP_005265273.1:p.Ser132Arg
NM_015896.4:c.631A>C MANE Select	NP_056980.2:p.Ser211Arg
NM_001308379.2:c.599+131A>C	NP_001295308.1:n.599+131A>C