Canonical Allele Identifier: CA399605163

Gene: MLX

Linked Data

• dbSNP Id: rs1245733780
• gnomAD v2: 17-40723579-T-G
• gnomAD v4: 17-42571561-T-G
• MyVariant Identifiers: chr17:g.40723579T>G (hg19) ; chr17:g.42571561T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571561T>G , CM000679.2:g.42571561T>G	GRCh38
NC_000017.10:g.40723579T>G , CM000679.1:g.40723579T>G	GRCh37
NC_000017.9:g.37977105T>G	NCBI36
NG_029442.1:g.9502T>G
NG_031960.1:g.11271A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.693T>G MANE Select	ENSP00000416627.1:p.Ile231Met
ENST00000246912.8:c.855T>G	ENSP00000246912.3:p.Ile285Met
ENST00000346833.8:c.603T>G	ENSP00000320913.3:p.Ile201Met
ENST00000435881.6:c.693T>G	ENSP00000416627.1:p.Ile231Met
ENST00000585403.5:n.900T>G
ENST00000588320.1:n.1169T>G
ENST00000590050.5:n.859T>G
NM_170607.2:c.855T>G	NP_733752.1:p.Ile285Met
NM_198204.1:c.693T>G	NP_937847.1:p.Ile231Met
NM_198205.1:c.603T>G	NP_937848.1:p.Ile201Met
NM_198204.2:c.693T>G MANE Select	NP_937847.1:p.Ile231Met
NM_170607.3:c.855T>G	NP_733752.1:p.Ile285Met
NM_198205.2:c.603T>G	NP_937848.1:p.Ile201Met