Canonical Allele Identifier: CA2260544065
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571373C= , CM000679.2:g.42571373C= GRCh38
NC_000017.10:g.40723391C= , CM000679.1:g.40723391C= GRCh37
NC_000017.9:g.37976917C= NCBI36
NG_029442.1:g.9314C=
NG_031960.1:g.11459G=

Transcript Alleles

HGVS Amino-acid change
ENST00000435881.7:c.679-174C= MANE Select ENSP00000416627.1:n.679-174C=
ENST00000246912.8:c.841-174C= ENSP00000246912.3:n.841-174C=
ENST00000346833.8:c.589-174C= ENSP00000320913.3:n.589-174C=
ENST00000435881.6:c.679-174C= ENSP00000416627.1:n.679-174C=
ENST00000585403.5:n.886-174C=
ENST00000588320.1:n.1155-174C=
ENST00000590050.5:n.845-174C=
NM_170607.2:c.841-174C= NP_733752.1:n.841-174C=
NM_198204.1:c.679-174C= NP_937847.1:n.679-174C=
NM_198205.1:c.589-174C= NP_937848.1:n.589-174C=
NM_198204.2:c.679-174C= MANE Select NP_937847.1:n.679-174C=
NM_170607.3:c.841-174C= NP_733752.1:n.841-174C=
NM_198205.2:c.589-174C= NP_937848.1:n.589-174C=