Canonical Allele Identifier: CA2576276458

Gene: MLX

Linked Data

• gnomAD v4: 17-42571654-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571654A>G , CM000679.2:g.42571654A>G	GRCh38
NC_000017.10:g.40723672A>G , CM000679.1:g.40723672A>G	GRCh37
NC_000017.9:g.37977198A>G	NCBI36
NG_029442.1:g.9595A>G
NG_031960.1:g.11178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*51A>G MANE Select	ENSP00000416627.1:n.*51A>G
ENST00000246912.8:c.*51A>G	ENSP00000246912.3:n.*51A>G
ENST00000346833.8:c.*51A>G	ENSP00000320913.3:n.*51A>G
ENST00000435881.6:c.*51A>G	ENSP00000416627.1:n.*51A>G
ENST00000585403.5:n.993A>G
ENST00000588320.1:n.1262A>G
ENST00000590050.5:n.952A>G
NM_170607.2:c.*51A>G	NP_733752.1:n.*51A>G
NM_198204.1:c.*51A>G	NP_937847.1:n.*51A>G
NM_198205.1:c.*51A>G	NP_937848.1:n.*51A>G
NM_198204.2:c.*51A>G MANE Select	NP_937847.1:n.*51A>G
NM_170607.3:c.*51A>G	NP_733752.1:n.*51A>G
NM_198205.2:c.*51A>G	NP_937848.1:n.*51A>G