Canonical Allele Identifier: CA2637983132

Gene: MLX

Linked Data

• gnomAD v4: 17-42571626-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571627del , CM000679.2:g.42571627del	GRCh38
NC_000017.10:g.40723645del , CM000679.1:g.40723645del	GRCh37
NC_000017.9:g.37977171del	NCBI36
NG_029442.1:g.9568del
NG_031960.1:g.11205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*24del MANE Select	ENSP00000416627.1:n.*24del
ENST00000246912.8:c.*24del	ENSP00000246912.3:n.*24del
ENST00000346833.8:c.*24del	ENSP00000320913.3:n.*24del
ENST00000435881.6:c.*24del	ENSP00000416627.1:n.*24del
ENST00000585403.5:n.966del
ENST00000588320.1:n.1235del
ENST00000590050.5:n.925del
NM_170607.2:c.*24del	NP_733752.1:n.*24del
NM_198204.1:c.*24del	NP_937847.1:n.*24del
NM_198205.1:c.*24del	NP_937848.1:n.*24del
NM_198204.2:c.*24del MANE Select	NP_937847.1:n.*24del
NM_170607.3:c.*24del	NP_733752.1:n.*24del
NM_198205.2:c.*24del	NP_937848.1:n.*24del