Canonical Allele Identifier: CA2518898869
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571731T>A , CM000679.2:g.42571731T>A GRCh38
NC_000017.10:g.40723749T>A , CM000679.1:g.40723749T>A GRCh37
NC_000017.9:g.37977275T>A NCBI36
NG_029442.1:g.9672T>A
NG_031960.1:g.11101A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*128T>A MANE Select ENSP00000416627.1:n.*128T>A
ENST00000246912.8:c.*128T>A ENSP00000246912.3:n.*128T>A
ENST00000346833.8:c.*128T>A ENSP00000320913.3:n.*128T>A
ENST00000435881.6:c.*128T>A ENSP00000416627.1:n.*128T>A
ENST00000588320.1:n.1339T>A
ENST00000590050.5:n.1029T>A
NM_170607.2:c.*128T>A NP_733752.1:n.*128T>A
NM_198204.1:c.*128T>A NP_937847.1:n.*128T>A
NM_198205.1:c.*128T>A NP_937848.1:n.*128T>A
NM_198204.2:c.*128T>A MANE Select NP_937847.1:n.*128T>A
NM_170607.3:c.*128T>A NP_733752.1:n.*128T>A
NM_198205.2:c.*128T>A NP_937848.1:n.*128T>A