Canonical Allele Identifier: CA2260544161

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571566T= , CM000679.2:g.42571566T=	GRCh38
NC_000017.10:g.40723584T= , CM000679.1:g.40723584T=	GRCh37
NC_000017.9:g.37977110T=	NCBI36
NG_029442.1:g.9507T=
NG_031960.1:g.11266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.698T= MANE Select	ENSP00000416627.1:p.Ile233=
ENST00000246912.8:c.860T=	ENSP00000246912.3:p.Ile287=
ENST00000346833.8:c.608T=	ENSP00000320913.3:p.Ile203=
ENST00000435881.6:c.698T=	ENSP00000416627.1:p.Ile233=
ENST00000585403.5:n.905T=
ENST00000588320.1:n.1174T=
ENST00000590050.5:n.864T=
NM_170607.2:c.860T=	NP_733752.1:p.Ile287=
NM_198204.1:c.698T=	NP_937847.1:p.Ile233=
NM_198205.1:c.608T=	NP_937848.1:p.Ile203=
NM_198204.2:c.698T= MANE Select	NP_937847.1:p.Ile233=
NM_170607.3:c.860T=	NP_733752.1:p.Ile287=
NM_198205.2:c.608T=	NP_937848.1:p.Ile203=