Canonical Allele Identifier: CA2260544234
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571686T= , CM000679.2:g.42571686T= GRCh38
NC_000017.10:g.40723704T= , CM000679.1:g.40723704T= GRCh37
NC_000017.9:g.37977230T= NCBI36
NG_029442.1:g.9627T=
NG_031960.1:g.11146A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*83T= MANE Select ENSP00000416627.1:n.*83T=
ENST00000246912.8:c.*83T= ENSP00000246912.3:n.*83T=
ENST00000346833.8:c.*83T= ENSP00000320913.3:n.*83T=
ENST00000435881.6:c.*83T= ENSP00000416627.1:n.*83T=
ENST00000585403.5:n.1025T=
ENST00000588320.1:n.1294T=
ENST00000590050.5:n.984T=
NM_170607.2:c.*83T= NP_733752.1:n.*83T=
NM_198204.1:c.*83T= NP_937847.1:n.*83T=
NM_198205.1:c.*83T= NP_937848.1:n.*83T=
NM_198204.2:c.*83T= MANE Select NP_937847.1:n.*83T=
NM_170607.3:c.*83T= NP_733752.1:n.*83T=
NM_198205.2:c.*83T= NP_937848.1:n.*83T=