Canonical Allele Identifier: CA919843265

Gene: MLX

Linked Data

• dbSNP Id: rs1567910093

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571632_42571633insCTTGTTGGCTGT , CM000679.2:g.42571632_42571633insCTTGTTGGCTGT	GRCh38
NC_000017.10:g.40723650_40723651insCTTGTTGGCTGT , CM000679.1:g.40723650_40723651insCTTGTTGGCTGT	GRCh37
NC_000017.9:g.37977176_37977177insCTTGTTGGCTGT	NCBI36
NG_029442.1:g.9573_9574insCTTGTTGGCTGT
NG_031960.1:g.11199_11200insACAGCCAACAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*29_*30insCTTGTTGGCTGT MANE Select	ENSP00000416627.1:n.*29_*30insCTTGTTGGCTGT
ENST00000246912.8:c.*29_*30insCTTGTTGGCTGT	ENSP00000246912.3:n.*29_*30insCTTGTTGGCTGT
ENST00000346833.8:c.*29_*30insCTTGTTGGCTGT	ENSP00000320913.3:n.*29_*30insCTTGTTGGCTGT
ENST00000435881.6:c.*29_*30insCTTGTTGGCTGT	ENSP00000416627.1:n.*29_*30insCTTGTTGGCTGT
ENST00000585403.5:n.971_972insCTTGTTGGCTGT
ENST00000588320.1:n.1240_1241insCTTGTTGGCTGT
ENST00000590050.5:n.930_931insCTTGTTGGCTGT
NM_170607.2:c.*29_*30insCTTGTTGGCTGT	NP_733752.1:n.*29_*30insCTTGTTGGCTGT
NM_198204.1:c.*29_*30insCTTGTTGGCTGT	NP_937847.1:n.*29_*30insCTTGTTGGCTGT
NM_198205.1:c.*29_*30insCTTGTTGGCTGT	NP_937848.1:n.*29_*30insCTTGTTGGCTGT
NM_198204.2:c.*29_*30insCTTGTTGGCTGT MANE Select	NP_937847.1:n.*29_*30insCTTGTTGGCTGT
NM_170607.3:c.*29_*30insCTTGTTGGCTGT	NP_733752.1:n.*29_*30insCTTGTTGGCTGT
NM_198205.2:c.*29_*30insCTTGTTGGCTGT	NP_937848.1:n.*29_*30insCTTGTTGGCTGT