Canonical Allele Identifier: CA2260544167
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571576G= , CM000679.2:g.42571576G= GRCh38
NC_000017.10:g.40723594G= , CM000679.1:g.40723594G= GRCh37
NC_000017.9:g.37977120G= NCBI36
NG_029442.1:g.9517G=
NG_031960.1:g.11256C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.708G= MANE Select ENSP00000416627.1:p.Leu236=
ENST00000246912.8:c.870G= ENSP00000246912.3:p.Leu290=
ENST00000346833.8:c.618G= ENSP00000320913.3:p.Leu206=
ENST00000435881.6:c.708G= ENSP00000416627.1:p.Leu236=
ENST00000585403.5:n.915G=
ENST00000588320.1:n.1184G=
ENST00000590050.5:n.874G=
NM_170607.2:c.870G= NP_733752.1:p.Leu290=
NM_198204.1:c.708G= NP_937847.1:p.Leu236=
NM_198205.1:c.618G= NP_937848.1:p.Leu206=
NM_198204.2:c.708G= MANE Select NP_937847.1:p.Leu236=
NM_170607.3:c.870G= NP_733752.1:p.Leu290=
NM_198205.2:c.618G= NP_937848.1:p.Leu206=