Canonical Allele Identifier: CA2260544169

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571578A= , CM000679.2:g.42571578A=	GRCh38
NC_000017.10:g.40723596A= , CM000679.1:g.40723596A=	GRCh37
NC_000017.9:g.37977122A=	NCBI36
NG_029442.1:g.9519A=
NG_031960.1:g.11254T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.710A= MANE Select	ENSP00000416627.1:p.His237=
ENST00000246912.8:c.872A=	ENSP00000246912.3:p.His291=
ENST00000346833.8:c.620A=	ENSP00000320913.3:p.His207=
ENST00000435881.6:c.710A=	ENSP00000416627.1:p.His237=
ENST00000585403.5:n.917A=
ENST00000588320.1:n.1186A=
ENST00000590050.5:n.876A=
NM_170607.2:c.872A=	NP_733752.1:p.His291=
NM_198204.1:c.710A=	NP_937847.1:p.His237=
NM_198205.1:c.620A=	NP_937848.1:p.His207=
NM_198204.2:c.710A= MANE Select	NP_937847.1:p.His237=
NM_170607.3:c.872A=	NP_733752.1:p.His291=
NM_198205.2:c.620A=	NP_937848.1:p.His207=