Canonical Allele Identifier: CA2540305531

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571732T>G , CM000679.2:g.42571732T>G	GRCh38
NC_000017.10:g.40723750T>G , CM000679.1:g.40723750T>G	GRCh37
NC_000017.9:g.37977276T>G	NCBI36
NG_029442.1:g.9673T>G
NG_031960.1:g.11100A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*129T>G MANE Select	ENSP00000416627.1:n.*129T>G
ENST00000246912.8:c.*129T>G	ENSP00000246912.3:n.*129T>G
ENST00000346833.8:c.*129T>G	ENSP00000320913.3:n.*129T>G
ENST00000435881.6:c.*129T>G	ENSP00000416627.1:n.*129T>G
ENST00000588320.1:n.1340T>G
ENST00000590050.5:n.1030T>G
NM_170607.2:c.*129T>G	NP_733752.1:n.*129T>G
NM_198204.1:c.*129T>G	NP_937847.1:n.*129T>G
NM_198205.1:c.*129T>G	NP_937848.1:n.*129T>G
NM_198204.2:c.*129T>G MANE Select	NP_937847.1:n.*129T>G
NM_170607.3:c.*129T>G	NP_733752.1:n.*129T>G
NM_198205.2:c.*129T>G	NP_937848.1:n.*129T>G