Canonical Allele Identifier: CA2637983189

Gene: MLX

Linked Data

• gnomAD v4: 17-42571734-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571739del , CM000679.2:g.42571739del	GRCh38
NC_000017.10:g.40723757del , CM000679.1:g.40723757del	GRCh37
NC_000017.9:g.37977283del	NCBI36
NG_029442.1:g.9680del
NG_031960.1:g.11097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*136del MANE Select	ENSP00000416627.1:n.*136del
ENST00000246912.8:c.*136del	ENSP00000246912.3:n.*136del
ENST00000346833.8:c.*136del	ENSP00000320913.3:n.*136del
ENST00000435881.6:c.*136del	ENSP00000416627.1:n.*136del
ENST00000588320.1:n.1347del
ENST00000590050.5:n.1037del
NM_170607.2:c.*136del	NP_733752.1:n.*136del
NM_198204.1:c.*136del	NP_937847.1:n.*136del
NM_198205.1:c.*136del	NP_937848.1:n.*136del
NM_198204.2:c.*136del MANE Select	NP_937847.1:n.*136del
NM_170607.3:c.*136del	NP_733752.1:n.*136del
NM_198205.2:c.*136del	NP_937848.1:n.*136del