Canonical Allele Identifier: CA2260544243
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571696C= , CM000679.2:g.42571696C= GRCh38
NC_000017.10:g.40723714C= , CM000679.1:g.40723714C= GRCh37
NC_000017.9:g.37977240C= NCBI36
NG_029442.1:g.9637C=
NG_031960.1:g.11136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*93C= MANE Select ENSP00000416627.1:n.*93C=
ENST00000246912.8:c.*93C= ENSP00000246912.3:n.*93C=
ENST00000346833.8:c.*93C= ENSP00000320913.3:n.*93C=
ENST00000435881.6:c.*93C= ENSP00000416627.1:n.*93C=
ENST00000585403.5:n.1035C=
ENST00000588320.1:n.1304C=
ENST00000590050.5:n.994C=
NM_170607.2:c.*93C= NP_733752.1:n.*93C=
NM_198204.1:c.*93C= NP_937847.1:n.*93C=
NM_198205.1:c.*93C= NP_937848.1:n.*93C=
NM_198204.2:c.*93C= MANE Select NP_937847.1:n.*93C=
NM_170607.3:c.*93C= NP_733752.1:n.*93C=
NM_198205.2:c.*93C= NP_937848.1:n.*93C=