Canonical Allele Identifier: CA8578776

Gene: MLX

Linked Data

• dbSNP Id: rs548731086
• ExAC: 17:40723630 T / TGG
• gnomAD v2: 17-40723630-T-TGG
• gnomAD v3: 17-42571612-T-TGG
• gnomAD v4: 17-42571612-T-TGG
• MyVariant Identifiers: chr17:g.40723630_40723631insGG (hg19) ; chr17:g.42571612_42571613insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571613_42571614dup , CM000679.2:g.42571613_42571614dup	GRCh38
NC_000017.10:g.40723631_40723632dup , CM000679.1:g.40723631_40723632dup	GRCh37
NC_000017.9:g.37977157_37977158dup	NCBI36
NG_029442.1:g.9554_9555dup
NG_031960.1:g.11218_11219dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*10_*11dup MANE Select	ENSP00000416627.1:n.*10_*11dup
ENST00000246912.8:c.*10_*11dup	ENSP00000246912.3:n.*10_*11dup
ENST00000346833.8:c.*10_*11dup	ENSP00000320913.3:n.*10_*11dup
ENST00000435881.6:c.*10_*11dup	ENSP00000416627.1:n.*10_*11dup
ENST00000585403.5:n.952_953dup
ENST00000588320.1:n.1221_1222dup
ENST00000590050.5:n.911_912dup
NM_170607.2:c.*10_*11dup	NP_733752.1:n.*10_*11dup
NM_198204.1:c.*10_*11dup	NP_937847.1:n.*10_*11dup
NM_198205.1:c.*10_*11dup	NP_937848.1:n.*10_*11dup
NM_198204.2:c.*10_*11dup MANE Select	NP_937847.1:n.*10_*11dup
NM_170607.3:c.*10_*11dup	NP_733752.1:n.*10_*11dup
NM_198205.2:c.*10_*11dup	NP_937848.1:n.*10_*11dup