Canonical Allele Identifier: CA772121440

Gene: MLX

Linked Data

• dbSNP Id: rs1389738931
• gnomAD v4: 17-42571692-AC-A
• MyVariant Identifiers: chr17:g.40723711del (hg19) ; chr17:g.42571693del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571693del , CM000679.2:g.42571693del	GRCh38
NC_000017.10:g.40723711del , CM000679.1:g.40723711del	GRCh37
NC_000017.9:g.37977237del	NCBI36
NG_029442.1:g.9634del
NG_031960.1:g.11139del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*90del MANE Select	ENSP00000416627.1:n.*90del
ENST00000246912.8:c.*90del	ENSP00000246912.3:n.*90del
ENST00000346833.8:c.*90del	ENSP00000320913.3:n.*90del
ENST00000435881.6:c.*90del	ENSP00000416627.1:n.*90del
ENST00000585403.5:n.1032del
ENST00000588320.1:n.1301del
ENST00000590050.5:n.991del
NM_170607.2:c.*90del	NP_733752.1:n.*90del
NM_198204.1:c.*90del	NP_937847.1:n.*90del
NM_198205.1:c.*90del	NP_937848.1:n.*90del
NM_198204.2:c.*90del MANE Select	NP_937847.1:n.*90del
NM_170607.3:c.*90del	NP_733752.1:n.*90del
NM_198205.2:c.*90del	NP_937848.1:n.*90del