Canonical Allele Identifier: CA983840771

Gene: MLX

Linked Data

• dbSNP Id: rs2093033899
• gnomAD v3: 17-42571719-TC-T
• gnomAD v4: 17-42571719-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571720del , CM000679.2:g.42571720del	GRCh38
NC_000017.10:g.40723738del , CM000679.1:g.40723738del	GRCh37
NC_000017.9:g.37977264del	NCBI36
NG_029442.1:g.9661del
NG_031960.1:g.11112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*117del MANE Select	ENSP00000416627.1:n.*117del
ENST00000246912.8:c.*117del	ENSP00000246912.3:n.*117del
ENST00000346833.8:c.*117del	ENSP00000320913.3:n.*117del
ENST00000435881.6:c.*117del	ENSP00000416627.1:n.*117del
ENST00000585403.5:n.1059del
ENST00000588320.1:n.1328del
ENST00000590050.5:n.1018del
NM_170607.2:c.*117del	NP_733752.1:n.*117del
NM_198204.1:c.*117del	NP_937847.1:n.*117del
NM_198205.1:c.*117del	NP_937848.1:n.*117del
NM_198204.2:c.*117del MANE Select	NP_937847.1:n.*117del
NM_170607.3:c.*117del	NP_733752.1:n.*117del
NM_198205.2:c.*117del	NP_937848.1:n.*117del