Canonical Allele Identifier: CA399605347
Gene: MLX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571598T>A , CM000679.2:g.42571598T>A GRCh38
NC_000017.10:g.40723616T>A , CM000679.1:g.40723616T>A GRCh37
NC_000017.9:g.37977142T>A NCBI36
NG_029442.1:g.9539T>A
NG_031960.1:g.11234A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.730T>A MANE Select ENSP00000416627.1:p.Tyr244Asn
ENST00000246912.8:c.892T>A ENSP00000246912.3:p.Tyr298Asn
ENST00000346833.8:c.640T>A ENSP00000320913.3:p.Tyr214Asn
ENST00000435881.6:c.730T>A ENSP00000416627.1:p.Tyr244Asn
ENST00000585403.5:n.937T>A
ENST00000588320.1:n.1206T>A
ENST00000590050.5:n.896T>A
NM_170607.2:c.892T>A NP_733752.1:p.Tyr298Asn
NM_198204.1:c.730T>A NP_937847.1:p.Tyr244Asn
NM_198205.1:c.640T>A NP_937848.1:p.Tyr214Asn
NM_198204.2:c.730T>A MANE Select NP_937847.1:p.Tyr244Asn
NM_170607.3:c.892T>A NP_733752.1:p.Tyr298Asn
NM_198205.2:c.640T>A NP_937848.1:p.Tyr214Asn