Canonical Allele Identifier: CA500068408

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723579T>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.693T>A MANE Select	ENSP00000416627.1:p.Ile231=
ENST00000246912.8:c.855T>A	ENSP00000246912.3:p.Ile285=
ENST00000346833.8:c.603T>A	ENSP00000320913.3:p.Ile201=
ENST00000435881.6:c.693T>A	ENSP00000416627.1:p.Ile231=
ENST00000585403.5:n.900T>A
ENST00000588320.1:n.1169T>A
ENST00000590050.5:n.859T>A
NM_170607.2:c.855T>A	NP_733752.1:p.Ile285=
NM_198204.1:c.693T>A	NP_937847.1:p.Ile231=
NM_198205.1:c.603T>A	NP_937848.1:p.Ile201=
NM_198204.2:c.693T>A MANE Select	NP_937847.1:p.Ile231=
NM_170607.3:c.855T>A	NP_733752.1:p.Ile285=
NM_198205.2:c.603T>A	NP_937848.1:p.Ile201=