Canonical Allele Identifier: CA2260544163

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571570C= , CM000679.2:g.42571570C=	GRCh38
NC_000017.10:g.40723588C= , CM000679.1:g.40723588C=	GRCh37
NC_000017.9:g.37977114C=	NCBI36
NG_029442.1:g.9511C=
NG_031960.1:g.11262G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.702C= MANE Select	ENSP00000416627.1:p.Gly234=
ENST00000246912.8:c.864C=	ENSP00000246912.3:p.Gly288=
ENST00000346833.8:c.612C=	ENSP00000320913.3:p.Gly204=
ENST00000435881.6:c.702C=	ENSP00000416627.1:p.Gly234=
ENST00000585403.5:n.909C=
ENST00000588320.1:n.1178C=
ENST00000590050.5:n.868C=
NM_170607.2:c.864C=	NP_733752.1:p.Gly288=
NM_198204.1:c.702C=	NP_937847.1:p.Gly234=
NM_198205.1:c.612C=	NP_937848.1:p.Gly204=
NM_198204.2:c.702C= MANE Select	NP_937847.1:p.Gly234=
NM_170607.3:c.864C=	NP_733752.1:p.Gly288=
NM_198205.2:c.612C=	NP_937848.1:p.Gly204=