Canonical Allele Identifier: CA983840713
Gene: MLX HGNC NCBI

Linked Data

dbSNP Id: rs2093033050

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571590del , CM000679.2:g.42571590del GRCh38
NC_000017.10:g.40723608del , CM000679.1:g.40723608del GRCh37
NC_000017.9:g.37977134del NCBI36
NG_029442.1:g.9531del
NG_031960.1:g.11246del

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.722del MANE Select ENSP00000416627.1:p.Asn241ThrfsTer?
ENST00000246912.8:c.884del ENSP00000246912.3:p.Asn295ThrfsTer?
ENST00000346833.8:c.632del ENSP00000320913.3:p.Asn211ThrfsTer?
ENST00000435881.6:c.722del ENSP00000416627.1:p.Asn241ThrfsTer?
ENST00000585403.5:n.929del
ENST00000588320.1:n.1198del
ENST00000590050.5:n.888del
NM_170607.2:c.884del NP_733752.1:p.Asn295ThrfsTer?
NM_198204.1:c.722del NP_937847.1:p.Asn241ThrfsTer?
NM_198205.1:c.632del NP_937848.1:p.Asn211ThrfsTer?
NM_198204.2:c.722del MANE Select NP_937847.1:p.Asn241ThrfsTer?
NM_170607.3:c.884del NP_733752.1:p.Asn295ThrfsTer?
NM_198205.2:c.632del NP_937848.1:p.Asn211ThrfsTer?