Canonical Allele Identifier: CA2260544262

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571740C= , CM000679.2:g.42571740C=	GRCh38
NC_000017.10:g.40723758C= , CM000679.1:g.40723758C=	GRCh37
NC_000017.9:g.37977284C=	NCBI36
NG_029442.1:g.9681C=
NG_031960.1:g.11092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*137C= MANE Select	ENSP00000416627.1:n.*137C=
ENST00000246912.8:c.*137C=	ENSP00000246912.3:n.*137C=
ENST00000346833.8:c.*137C=	ENSP00000320913.3:n.*137C=
ENST00000435881.6:c.*137C=	ENSP00000416627.1:n.*137C=
ENST00000588320.1:n.1348C=
ENST00000590050.5:n.1038C=
NM_170607.2:c.*137C=	NP_733752.1:n.*137C=
NM_198204.1:c.*137C=	NP_937847.1:n.*137C=
NM_198205.1:c.*137C=	NP_937848.1:n.*137C=
NM_198204.2:c.*137C= MANE Select	NP_937847.1:n.*137C=
NM_170607.3:c.*137C=	NP_733752.1:n.*137C=
NM_198205.2:c.*137C=	NP_937848.1:n.*137C=