Canonical Allele Identifier: CA290776888

Gene: MLX

Linked Data

• dbSNP Id: rs1016403222
• gnomAD v4: 17-42571734-G-T
• MyVariant Identifiers: chr17:g.40723752G>T (hg19) ; chr17:g.42571734G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571734G>T , CM000679.2:g.42571734G>T	GRCh38
NC_000017.10:g.40723752G>T , CM000679.1:g.40723752G>T	GRCh37
NC_000017.9:g.37977278G>T	NCBI36
NG_029442.1:g.9675G>T
NG_031960.1:g.11098C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*131G>T MANE Select	ENSP00000416627.1:n.*131G>T
ENST00000246912.8:c.*131G>T	ENSP00000246912.3:n.*131G>T
ENST00000346833.8:c.*131G>T	ENSP00000320913.3:n.*131G>T
ENST00000435881.6:c.*131G>T	ENSP00000416627.1:n.*131G>T
ENST00000588320.1:n.1342G>T
ENST00000590050.5:n.1032G>T
NM_170607.2:c.*131G>T	NP_733752.1:n.*131G>T
NM_198204.1:c.*131G>T	NP_937847.1:n.*131G>T
NM_198205.1:c.*131G>T	NP_937848.1:n.*131G>T
NM_198204.2:c.*131G>T MANE Select	NP_937847.1:n.*131G>T
NM_170607.3:c.*131G>T	NP_733752.1:n.*131G>T
NM_198205.2:c.*131G>T	NP_937848.1:n.*131G>T