Canonical Allele Identifier: CA2260544177

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571591C= , CM000679.2:g.42571591C=	GRCh38
NC_000017.10:g.40723609C= , CM000679.1:g.40723609C=	GRCh37
NC_000017.9:g.37977135C=	NCBI36
NG_029442.1:g.9532C=
NG_031960.1:g.11241G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.723C= MANE Select	ENSP00000416627.1:p.Asn241=
ENST00000246912.8:c.885C=	ENSP00000246912.3:p.Asn295=
ENST00000346833.8:c.633C=	ENSP00000320913.3:p.Asn211=
ENST00000435881.6:c.723C=	ENSP00000416627.1:p.Asn241=
ENST00000585403.5:n.930C=
ENST00000588320.1:n.1199C=
ENST00000590050.5:n.889C=
NM_170607.2:c.885C=	NP_733752.1:p.Asn295=
NM_198204.1:c.723C=	NP_937847.1:p.Asn241=
NM_198205.1:c.633C=	NP_937848.1:p.Asn211=
NM_198204.2:c.723C= MANE Select	NP_937847.1:p.Asn241=
NM_170607.3:c.885C=	NP_733752.1:p.Asn295=
NM_198205.2:c.633C=	NP_937848.1:p.Asn211=