Canonical Allele Identifier: CA2260544154
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571551T= , CM000679.2:g.42571551T= GRCh38
NC_000017.10:g.40723569T= , CM000679.1:g.40723569T= GRCh37
NC_000017.9:g.37977095T= NCBI36
NG_029442.1:g.9492T=
NG_031960.1:g.11281A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.683T= MANE Select ENSP00000416627.1:p.Leu228=
ENST00000246912.8:c.845T= ENSP00000246912.3:p.Leu282=
ENST00000346833.8:c.593T= ENSP00000320913.3:p.Leu198=
ENST00000435881.6:c.683T= ENSP00000416627.1:p.Leu228=
ENST00000585403.5:n.890T=
ENST00000588320.1:n.1159T=
ENST00000590050.5:n.849T=
NM_170607.2:c.845T= NP_733752.1:p.Leu282=
NM_198204.1:c.683T= NP_937847.1:p.Leu228=
NM_198205.1:c.593T= NP_937848.1:p.Leu198=
NM_198204.2:c.683T= MANE Select NP_937847.1:p.Leu228=
NM_170607.3:c.845T= NP_733752.1:p.Leu282=
NM_198205.2:c.593T= NP_937848.1:p.Leu198=