Canonical Allele Identifier: CA983840755
Gene: MLX HGNC NCBI

Linked Data

dbSNP Id: rs2093033515

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571643_42571645del , CM000679.2:g.42571643_42571645del GRCh38
NC_000017.10:g.40723661_40723663del , CM000679.1:g.40723661_40723663del GRCh37
NC_000017.9:g.37977187_37977189del NCBI36
NG_029442.1:g.9584_9586del
NG_031960.1:g.11187_11189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*40_*42del MANE Select ENSP00000416627.1:n.*40_*42del
ENST00000246912.8:c.*40_*42del ENSP00000246912.3:n.*40_*42del
ENST00000346833.8:c.*40_*42del ENSP00000320913.3:n.*40_*42del
ENST00000435881.6:c.*40_*42del ENSP00000416627.1:n.*40_*42del
ENST00000585403.5:n.982_984del
ENST00000588320.1:n.1251_1253del
ENST00000590050.5:n.941_943del
NM_170607.2:c.*40_*42del NP_733752.1:n.*40_*42del
NM_198204.1:c.*40_*42del NP_937847.1:n.*40_*42del
NM_198205.1:c.*40_*42del NP_937848.1:n.*40_*42del
NM_198204.2:c.*40_*42del MANE Select NP_937847.1:n.*40_*42del
NM_170607.3:c.*40_*42del NP_733752.1:n.*40_*42del
NM_198205.2:c.*40_*42del NP_937848.1:n.*40_*42del