Canonical Allele Identifier: CA413498269

Gene: ZMYM3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71241095G>A , CM000685.2:g.71241095G>A	GRCh38
NC_000023.10:g.70460945G>A , CM000685.1:g.70460945G>A	GRCh37
NC_000023.9:g.70377670G>A	NCBI36
NG_016407.1:g.19103C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314425.9:c.3934C>T MANE Select	ENSP00000322845.5:p.Arg1312Trp
ENST00000373984.7:c.3664C>T	ENSP00000363096.3:p.Arg1222Trp
ENST00000373988.5:c.3940C>T	ENSP00000363100.1:p.Arg1314Trp
ENST00000373998.5:c.3898C>T	ENSP00000363110.1:p.Arg1300Trp
ENST00000489332.1:n.4254C>T
NM_001171162.1:c.3898C>T	NP_001164633.1:p.Arg1300Trp
NM_005096.3:c.3934C>T	NP_005087.1:p.Arg1312Trp
NM_201599.2:c.3934C>T	NP_963893.1:p.Arg1312Trp
XM_005262309.2:c.3934C>T	XP_005262366.1:p.Arg1312Trp
XM_005262310.1:c.3898C>T	XP_005262367.1:p.Arg1300Trp
XM_011531062.1:c.3934C>T	XP_011529364.1:p.Arg1312Trp
XM_005262309.4:c.3934C>T	XP_005262366.1:p.Arg1312Trp
XM_005262310.3:c.3898C>T	XP_005262367.1:p.Arg1300Trp
XM_011531062.3:c.3934C>T	XP_011529364.1:p.Arg1312Trp
NM_201599.3:c.3934C>T MANE Select	NP_963893.1:p.Arg1312Trp