Canonical Allele Identifier: CA772121439

Gene: MLX

Linked Data

• dbSNP Id: rs1354246648
• MyVariant Identifiers: chr17:g.40723707_40723708insCTACAACAC (hg19) ; chr17:g.42571689_42571690insCTACAACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571692_42571700dup , CM000679.2:g.42571692_42571700dup	GRCh38
NC_000017.10:g.40723710_40723718dup , CM000679.1:g.40723710_40723718dup	GRCh37
NC_000017.9:g.37977236_37977244dup	NCBI36
NG_029442.1:g.9633_9641dup
NG_031960.1:g.11134_11142dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*89_*97dup MANE Select	ENSP00000416627.1:n.*89_*97dup
ENST00000246912.8:c.*89_*97dup	ENSP00000246912.3:n.*89_*97dup
ENST00000346833.8:c.*89_*97dup	ENSP00000320913.3:n.*89_*97dup
ENST00000435881.6:c.*89_*97dup	ENSP00000416627.1:n.*89_*97dup
ENST00000585403.5:n.1031_1039dup
ENST00000588320.1:n.1300_1308dup
ENST00000590050.5:n.990_998dup
NM_170607.2:c.*89_*97dup	NP_733752.1:n.*89_*97dup
NM_198204.1:c.*89_*97dup	NP_937847.1:n.*89_*97dup
NM_198205.1:c.*89_*97dup	NP_937848.1:n.*89_*97dup
NM_198204.2:c.*89_*97dup MANE Select	NP_937847.1:n.*89_*97dup
NM_170607.3:c.*89_*97dup	NP_733752.1:n.*89_*97dup
NM_198205.2:c.*89_*97dup	NP_937848.1:n.*89_*97dup