Canonical Allele Identifier: CA399605211

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723590T>A (hg19) ; chr17:g.42571572T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571572T>A , CM000679.2:g.42571572T>A	GRCh38
NC_000017.10:g.40723590T>A , CM000679.1:g.40723590T>A	GRCh37
NC_000017.9:g.37977116T>A	NCBI36
NG_029442.1:g.9513T>A
NG_031960.1:g.11260A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.704T>A MANE Select	ENSP00000416627.1:p.Val235Asp
ENST00000246912.8:c.866T>A	ENSP00000246912.3:p.Val289Asp
ENST00000346833.8:c.614T>A	ENSP00000320913.3:p.Val205Asp
ENST00000435881.6:c.704T>A	ENSP00000416627.1:p.Val235Asp
ENST00000585403.5:n.911T>A
ENST00000588320.1:n.1180T>A
ENST00000590050.5:n.870T>A
NM_170607.2:c.866T>A	NP_733752.1:p.Val289Asp
NM_198204.1:c.704T>A	NP_937847.1:p.Val235Asp
NM_198205.1:c.614T>A	NP_937848.1:p.Val205Asp
NM_198204.2:c.704T>A MANE Select	NP_937847.1:p.Val235Asp
NM_170607.3:c.866T>A	NP_733752.1:p.Val289Asp
NM_198205.2:c.614T>A	NP_937848.1:p.Val205Asp