Canonical Allele Identifier: CA399605287
Gene: MLX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571587A>T , CM000679.2:g.42571587A>T GRCh38
NC_000017.10:g.40723605A>T , CM000679.1:g.40723605A>T GRCh37
NC_000017.9:g.37977131A>T NCBI36
NG_029442.1:g.9528A>T
NG_031960.1:g.11245T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.719A>T MANE Select ENSP00000416627.1:p.Lys240Ile
ENST00000246912.8:c.881A>T ENSP00000246912.3:p.Lys294Ile
ENST00000346833.8:c.629A>T ENSP00000320913.3:p.Lys210Ile
ENST00000435881.6:c.719A>T ENSP00000416627.1:p.Lys240Ile
ENST00000585403.5:n.926A>T
ENST00000588320.1:n.1195A>T
ENST00000590050.5:n.885A>T
NM_170607.2:c.881A>T NP_733752.1:p.Lys294Ile
NM_198204.1:c.719A>T NP_937847.1:p.Lys240Ile
NM_198205.1:c.629A>T NP_937848.1:p.Lys210Ile
NM_198204.2:c.719A>T MANE Select NP_937847.1:p.Lys240Ile
NM_170607.3:c.881A>T NP_733752.1:p.Lys294Ile
NM_198205.2:c.629A>T NP_937848.1:p.Lys210Ile