Canonical Allele Identifier: CA2260544210
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571642_42571645delinsCCTT , CM000679.2:g.42571642_42571645delinsCCTT GRCh38
NC_000017.10:g.40723660_40723663delinsCCTT , CM000679.1:g.40723660_40723663delinsCCTT GRCh37
NC_000017.9:g.37977186_37977189delinsCCTT NCBI36
NG_029442.1:g.9583_9586delinsCCTT
NG_031960.1:g.11187_11190delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*39_*42delinsCCTT MANE Select ENSP00000416627.1:n.*39_*42delinsCCTT
ENST00000246912.8:c.*39_*42delinsCCTT ENSP00000246912.3:n.*39_*42delinsCCTT
ENST00000346833.8:c.*39_*42delinsCCTT ENSP00000320913.3:n.*39_*42delinsCCTT
ENST00000435881.6:c.*39_*42delinsCCTT ENSP00000416627.1:n.*39_*42delinsCCTT
ENST00000585403.5:n.981_984delinsCCTT
ENST00000588320.1:n.1250_1253delinsCCTT
ENST00000590050.5:n.940_943delinsCCTT
NM_170607.2:c.*39_*42delinsCCTT NP_733752.1:n.*39_*42delinsCCTT
NM_198204.1:c.*39_*42delinsCCTT NP_937847.1:n.*39_*42delinsCCTT
NM_198205.1:c.*39_*42delinsCCTT NP_937848.1:n.*39_*42delinsCCTT
NM_198204.2:c.*39_*42delinsCCTT MANE Select NP_937847.1:n.*39_*42delinsCCTT
NM_170607.3:c.*39_*42delinsCCTT NP_733752.1:n.*39_*42delinsCCTT
NM_198205.2:c.*39_*42delinsCCTT NP_937848.1:n.*39_*42delinsCCTT