Canonical Allele Identifier: CA2260544213

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571645T= , CM000679.2:g.42571645T=	GRCh38
NC_000017.10:g.40723663T= , CM000679.1:g.40723663T=	GRCh37
NC_000017.9:g.37977189T=	NCBI36
NG_029442.1:g.9586T=
NG_031960.1:g.11187A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*42T= MANE Select	ENSP00000416627.1:n.*42T=
ENST00000246912.8:c.*42T=	ENSP00000246912.3:n.*42T=
ENST00000346833.8:c.*42T=	ENSP00000320913.3:n.*42T=
ENST00000435881.6:c.*42T=	ENSP00000416627.1:n.*42T=
ENST00000585403.5:n.984T=
ENST00000588320.1:n.1253T=
ENST00000590050.5:n.943T=
NM_170607.2:c.*42T=	NP_733752.1:n.*42T=
NM_198204.1:c.*42T=	NP_937847.1:n.*42T=
NM_198205.1:c.*42T=	NP_937848.1:n.*42T=
NM_198204.2:c.*42T= MANE Select	NP_937847.1:n.*42T=
NM_170607.3:c.*42T=	NP_733752.1:n.*42T=
NM_198205.2:c.*42T=	NP_937848.1:n.*42T=