Canonical Allele Identifier: CA2260544060
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571370_42571371delinsAC , CM000679.2:g.42571370_42571371delinsAC GRCh38
NC_000017.10:g.40723388_40723389delinsAC , CM000679.1:g.40723388_40723389delinsAC GRCh37
NC_000017.9:g.37976914_37976915delinsAC NCBI36
NG_029442.1:g.9311_9312delinsAC
NG_031960.1:g.11461_11462delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.679-177_679-176delinsAC MANE Select ENSP00000416627.1:n.679-177_679-176delinsAC
ENST00000246912.8:c.841-177_841-176delinsAC ENSP00000246912.3:n.841-177_841-176delinsAC
ENST00000346833.8:c.589-177_589-176delinsAC ENSP00000320913.3:n.589-177_589-176delinsAC
ENST00000435881.6:c.679-177_679-176delinsAC ENSP00000416627.1:n.679-177_679-176delinsAC
ENST00000585403.5:n.886-177_886-176delinsAC
ENST00000588320.1:n.1155-177_1155-176delinsAC
ENST00000590050.5:n.845-177_845-176delinsAC
NM_170607.2:c.841-177_841-176delinsAC NP_733752.1:n.841-177_841-176delinsAC
NM_198204.1:c.679-177_679-176delinsAC NP_937847.1:n.679-177_679-176delinsAC
NM_198205.1:c.589-177_589-176delinsAC NP_937848.1:n.589-177_589-176delinsAC
NM_198204.2:c.679-177_679-176delinsAC MANE Select NP_937847.1:n.679-177_679-176delinsAC
NM_170607.3:c.841-177_841-176delinsAC NP_733752.1:n.841-177_841-176delinsAC
NM_198205.2:c.589-177_589-176delinsAC NP_937848.1:n.589-177_589-176delinsAC