Canonical Allele Identifier: CA2809526366

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571636_42571638dup , CM000679.2:g.42571636_42571638dup	GRCh38
NC_000017.10:g.40723654_40723656dup , CM000679.1:g.40723654_40723656dup	GRCh37
NC_000017.9:g.37977180_37977182dup	NCBI36
NG_029442.1:g.9577_9579dup
NG_031960.1:g.11195_11197dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*33_*35dup MANE Select	ENSP00000416627.1:n.*33_*35dup
ENST00000246912.8:c.*33_*35dup	ENSP00000246912.3:n.*33_*35dup
ENST00000346833.8:c.*33_*35dup	ENSP00000320913.3:n.*33_*35dup
ENST00000435881.6:c.*33_*35dup	ENSP00000416627.1:n.*33_*35dup
ENST00000585403.5:n.975_977dup
ENST00000588320.1:n.1244_1246dup
ENST00000590050.5:n.934_936dup
NM_170607.2:c.*33_*35dup	NP_733752.1:n.*33_*35dup
NM_198204.1:c.*33_*35dup	NP_937847.1:n.*33_*35dup
NM_198205.1:c.*33_*35dup	NP_937848.1:n.*33_*35dup
NM_198204.2:c.*33_*35dup MANE Select	NP_937847.1:n.*33_*35dup
NM_170607.3:c.*33_*35dup	NP_733752.1:n.*33_*35dup
NM_198205.2:c.*33_*35dup	NP_937848.1:n.*33_*35dup