Canonical Allele Identifier: CA500068536

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723620G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571602G>A , CM000679.2:g.42571602G>A	GRCh38
NC_000017.10:g.40723620G>A , CM000679.1:g.40723620G>A	GRCh37
NC_000017.9:g.37977146G>A	NCBI36
NG_029442.1:g.9543G>A
NG_031960.1:g.11230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.734G>A MANE Select	ENSP00000416627.1:p.Ter245=
ENST00000246912.8:c.896G>A	ENSP00000246912.3:p.Ter299=
ENST00000346833.8:c.644G>A	ENSP00000320913.3:p.Ter215=
ENST00000435881.6:c.734G>A	ENSP00000416627.1:p.Ter245=
ENST00000585403.5:n.941G>A
ENST00000588320.1:n.1210G>A
ENST00000590050.5:n.900G>A
NM_170607.2:c.896G>A	NP_733752.1:p.Ter299=
NM_198204.1:c.734G>A	NP_937847.1:p.Ter245=
NM_198205.1:c.644G>A	NP_937848.1:p.Ter215=
NM_198204.2:c.734G>A MANE Select	NP_937847.1:p.Ter245=
NM_170607.3:c.896G>A	NP_733752.1:p.Ter299=
NM_198205.2:c.644G>A	NP_937848.1:p.Ter215=