Canonical Allele Identifier: CA10445752

Gene: ZMYM3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71248772G>A , CM000685.2:g.71248772G>A	GRCh38
NC_000023.10:g.70468622G>A , CM000685.1:g.70468622G>A	GRCh37
NC_000023.9:g.70385347G>A	NCBI36
NG_016407.1:g.11426C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314425.9:c.1651C>T MANE Select	ENSP00000322845.5:p.Arg551Cys
ENST00000373984.7:c.1657C>T	ENSP00000363096.3:p.Arg553Cys
ENST00000373988.5:c.1657C>T	ENSP00000363100.1:p.Arg553Cys
ENST00000373998.5:c.1651C>T	ENSP00000363110.1:p.Arg551Cys
ENST00000489332.1:n.1769C>T
NM_001171162.1:c.1651C>T	NP_001164633.1:p.Arg551Cys
NM_005096.3:c.1651C>T	NP_005087.1:p.Arg551Cys
NM_201599.2:c.1651C>T	NP_963893.1:p.Arg551Cys
XM_005262309.2:c.1651C>T	XP_005262366.1:p.Arg551Cys
XM_005262310.1:c.1651C>T	XP_005262367.1:p.Arg551Cys
XM_011531062.1:c.1651C>T	XP_011529364.1:p.Arg551Cys
XM_005262309.4:c.1651C>T	XP_005262366.1:p.Arg551Cys
XM_005262310.3:c.1651C>T	XP_005262367.1:p.Arg551Cys
XM_011531062.3:c.1651C>T	XP_011529364.1:p.Arg551Cys
NM_201599.3:c.1651C>T MANE Select	NP_963893.1:p.Arg551Cys