Canonical Allele Identifier: CA2637983172

Gene: MLX

Linked Data

• gnomAD v4: 17-42571707-G-GGTCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571708_42571713dup , CM000679.2:g.42571708_42571713dup	GRCh38
NC_000017.10:g.40723726_40723731dup , CM000679.1:g.40723726_40723731dup	GRCh37
NC_000017.9:g.37977252_37977257dup	NCBI36
NG_029442.1:g.9649_9654dup
NG_031960.1:g.11119_11124dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*105_*110dup MANE Select	ENSP00000416627.1:n.*105_*110dup
ENST00000246912.8:c.*105_*110dup	ENSP00000246912.3:n.*105_*110dup
ENST00000346833.8:c.*105_*110dup	ENSP00000320913.3:n.*105_*110dup
ENST00000435881.6:c.*105_*110dup	ENSP00000416627.1:n.*105_*110dup
ENST00000585403.5:n.1047_1052dup
ENST00000588320.1:n.1316_1321dup
ENST00000590050.5:n.1006_1011dup
NM_170607.2:c.*105_*110dup	NP_733752.1:n.*105_*110dup
NM_198204.1:c.*105_*110dup	NP_937847.1:n.*105_*110dup
NM_198205.1:c.*105_*110dup	NP_937848.1:n.*105_*110dup
NM_198204.2:c.*105_*110dup MANE Select	NP_937847.1:n.*105_*110dup
NM_170607.3:c.*105_*110dup	NP_733752.1:n.*105_*110dup
NM_198205.2:c.*105_*110dup	NP_937848.1:n.*105_*110dup