Canonical Allele Identifier: CA2576276454
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571626del , CM000679.2:g.42571626del GRCh38
NC_000017.10:g.40723644del , CM000679.1:g.40723644del GRCh37
NC_000017.9:g.37977170del NCBI36
NG_029442.1:g.9567del
NG_031960.1:g.11207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*23del MANE Select ENSP00000416627.1:n.*23del
ENST00000246912.8:c.*23del ENSP00000246912.3:n.*23del
ENST00000346833.8:c.*23del ENSP00000320913.3:n.*23del
ENST00000435881.6:c.*23del ENSP00000416627.1:n.*23del
ENST00000585403.5:n.965del
ENST00000588320.1:n.1234del
ENST00000590050.5:n.924del
NM_170607.2:c.*23del NP_733752.1:n.*23del
NM_198204.1:c.*23del NP_937847.1:n.*23del
NM_198205.1:c.*23del NP_937848.1:n.*23del
NM_198204.2:c.*23del MANE Select NP_937847.1:n.*23del
NM_170607.3:c.*23del NP_733752.1:n.*23del
NM_198205.2:c.*23del NP_937848.1:n.*23del