Canonical Allele Identifier: CA2809526365
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571615A>T , CM000679.2:g.42571615A>T GRCh38
NC_000017.10:g.40723633A>T , CM000679.1:g.40723633A>T GRCh37
NC_000017.9:g.37977159A>T NCBI36
NG_029442.1:g.9556A>T
NG_031960.1:g.11217T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*12A>T MANE Select ENSP00000416627.1:n.*12A>T
ENST00000246912.8:c.*12A>T ENSP00000246912.3:n.*12A>T
ENST00000346833.8:c.*12A>T ENSP00000320913.3:n.*12A>T
ENST00000435881.6:c.*12A>T ENSP00000416627.1:n.*12A>T
ENST00000585403.5:n.954A>T
ENST00000588320.1:n.1223A>T
ENST00000590050.5:n.913A>T
NM_170607.2:c.*12A>T NP_733752.1:n.*12A>T
NM_198204.1:c.*12A>T NP_937847.1:n.*12A>T
NM_198205.1:c.*12A>T NP_937848.1:n.*12A>T
NM_198204.2:c.*12A>T MANE Select NP_937847.1:n.*12A>T
NM_170607.3:c.*12A>T NP_733752.1:n.*12A>T
NM_198205.2:c.*12A>T NP_937848.1:n.*12A>T