Canonical Allele Identifier: CA2260544191

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571624G= , CM000679.2:g.42571624G=	GRCh38
NC_000017.10:g.40723642G= , CM000679.1:g.40723642G=	GRCh37
NC_000017.9:g.37977168G=	NCBI36
NG_029442.1:g.9565G=
NG_031960.1:g.11208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*21G= MANE Select	ENSP00000416627.1:n.*21G=
ENST00000246912.8:c.*21G=	ENSP00000246912.3:n.*21G=
ENST00000346833.8:c.*21G=	ENSP00000320913.3:n.*21G=
ENST00000435881.6:c.*21G=	ENSP00000416627.1:n.*21G=
ENST00000585403.5:n.963G=
ENST00000588320.1:n.1232G=
ENST00000590050.5:n.922G=
NM_170607.2:c.*21G=	NP_733752.1:n.*21G=
NM_198204.1:c.*21G=	NP_937847.1:n.*21G=
NM_198205.1:c.*21G=	NP_937848.1:n.*21G=
NM_198204.2:c.*21G= MANE Select	NP_937847.1:n.*21G=
NM_170607.3:c.*21G=	NP_733752.1:n.*21G=
NM_198205.2:c.*21G=	NP_937848.1:n.*21G=