Canonical Allele Identifier: CA983840773

Gene: MLX

Linked Data

• dbSNP Id: rs2093033910
• gnomAD v3: 17-42571722-A-T
• gnomAD v4: 17-42571722-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571722A>T , CM000679.2:g.42571722A>T	GRCh38
NC_000017.10:g.40723740A>T , CM000679.1:g.40723740A>T	GRCh37
NC_000017.9:g.37977266A>T	NCBI36
NG_029442.1:g.9663A>T
NG_031960.1:g.11110T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*119A>T MANE Select	ENSP00000416627.1:n.*119A>T
ENST00000246912.8:c.*119A>T	ENSP00000246912.3:n.*119A>T
ENST00000346833.8:c.*119A>T	ENSP00000320913.3:n.*119A>T
ENST00000435881.6:c.*119A>T	ENSP00000416627.1:n.*119A>T
ENST00000585403.5:n.1061A>T
ENST00000588320.1:n.1330A>T
ENST00000590050.5:n.1020A>T
NM_170607.2:c.*119A>T	NP_733752.1:n.*119A>T
NM_198204.1:c.*119A>T	NP_937847.1:n.*119A>T
NM_198205.1:c.*119A>T	NP_937848.1:n.*119A>T
NM_198204.2:c.*119A>T MANE Select	NP_937847.1:n.*119A>T
NM_170607.3:c.*119A>T	NP_733752.1:n.*119A>T
NM_198205.2:c.*119A>T	NP_937848.1:n.*119A>T