Canonical Allele Identifier: CA772121449

Gene: MLX

Linked Data

• dbSNP Id: rs1420847635
• gnomAD v3: 17-42571730-T-G
• gnomAD v4: 17-42571730-T-G
• MyVariant Identifiers: chr17:g.40723748T>G (hg19) ; chr17:g.42571730T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571730T>G , CM000679.2:g.42571730T>G	GRCh38
NC_000017.10:g.40723748T>G , CM000679.1:g.40723748T>G	GRCh37
NC_000017.9:g.37977274T>G	NCBI36
NG_029442.1:g.9671T>G
NG_031960.1:g.11102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*127T>G MANE Select	ENSP00000416627.1:n.*127T>G
ENST00000246912.8:c.*127T>G	ENSP00000246912.3:n.*127T>G
ENST00000346833.8:c.*127T>G	ENSP00000320913.3:n.*127T>G
ENST00000435881.6:c.*127T>G	ENSP00000416627.1:n.*127T>G
ENST00000588320.1:n.1338T>G
ENST00000590050.5:n.1028T>G
NM_170607.2:c.*127T>G	NP_733752.1:n.*127T>G
NM_198204.1:c.*127T>G	NP_937847.1:n.*127T>G
NM_198205.1:c.*127T>G	NP_937848.1:n.*127T>G
NM_198204.2:c.*127T>G MANE Select	NP_937847.1:n.*127T>G
NM_170607.3:c.*127T>G	NP_733752.1:n.*127T>G
NM_198205.2:c.*127T>G	NP_937848.1:n.*127T>G