Canonical Allele Identifier: CA2260544220
Gene: MLX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571655C= , CM000679.2:g.42571655C= GRCh38
NC_000017.10:g.40723673C= , CM000679.1:g.40723673C= GRCh37
NC_000017.9:g.37977199C= NCBI36
NG_029442.1:g.9596C=
NG_031960.1:g.11177G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.*52C= MANE Select ENSP00000416627.1:n.*52C=
ENST00000246912.8:c.*52C= ENSP00000246912.3:n.*52C=
ENST00000346833.8:c.*52C= ENSP00000320913.3:n.*52C=
ENST00000435881.6:c.*52C= ENSP00000416627.1:n.*52C=
ENST00000585403.5:n.994C=
ENST00000588320.1:n.1263C=
ENST00000590050.5:n.953C=
NM_170607.2:c.*52C= NP_733752.1:n.*52C=
NM_198204.1:c.*52C= NP_937847.1:n.*52C=
NM_198205.1:c.*52C= NP_937848.1:n.*52C=
NM_198204.2:c.*52C= MANE Select NP_937847.1:n.*52C=
NM_170607.3:c.*52C= NP_733752.1:n.*52C=
NM_198205.2:c.*52C= NP_937848.1:n.*52C=