Canonical Allele Identifier: CA2637983154

Gene: MLX

Linked Data

• gnomAD v4: 17-42571681-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571681G>A , CM000679.2:g.42571681G>A	GRCh38
NC_000017.10:g.40723699G>A , CM000679.1:g.40723699G>A	GRCh37
NC_000017.9:g.37977225G>A	NCBI36
NG_029442.1:g.9622G>A
NG_031960.1:g.11151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*78G>A MANE Select	ENSP00000416627.1:n.*78G>A
ENST00000246912.8:c.*78G>A	ENSP00000246912.3:n.*78G>A
ENST00000346833.8:c.*78G>A	ENSP00000320913.3:n.*78G>A
ENST00000435881.6:c.*78G>A	ENSP00000416627.1:n.*78G>A
ENST00000585403.5:n.1020G>A
ENST00000588320.1:n.1289G>A
ENST00000590050.5:n.979G>A
NM_170607.2:c.*78G>A	NP_733752.1:n.*78G>A
NM_198204.1:c.*78G>A	NP_937847.1:n.*78G>A
NM_198205.1:c.*78G>A	NP_937848.1:n.*78G>A
NM_198204.2:c.*78G>A MANE Select	NP_937847.1:n.*78G>A
NM_170607.3:c.*78G>A	NP_733752.1:n.*78G>A
NM_198205.2:c.*78G>A	NP_937848.1:n.*78G>A