Canonical Allele Identifier: CA2637983191

Gene: MLX

Linked Data

• gnomAD v4: 17-42571739-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571742del , CM000679.2:g.42571742del	GRCh38
NC_000017.10:g.40723760del , CM000679.1:g.40723760del	GRCh37
NC_000017.9:g.37977286del	NCBI36
NG_029442.1:g.9683del
NG_031960.1:g.11092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*139del MANE Select	ENSP00000416627.1:n.*139del
ENST00000246912.8:c.*139del	ENSP00000246912.3:n.*139del
ENST00000346833.8:c.*139del	ENSP00000320913.3:n.*139del
ENST00000435881.6:c.*139del	ENSP00000416627.1:n.*139del
ENST00000588320.1:n.1350del
ENST00000590050.5:n.1040del
NM_170607.2:c.*139del	NP_733752.1:n.*139del
NM_198204.1:c.*139del	NP_937847.1:n.*139del
NM_198205.1:c.*139del	NP_937848.1:n.*139del
NM_198204.2:c.*139del MANE Select	NP_937847.1:n.*139del
NM_170607.3:c.*139del	NP_733752.1:n.*139del
NM_198205.2:c.*139del	NP_937848.1:n.*139del