Canonical Allele Identifier: CA772121260

Gene: MLX

Linked Data

• dbSNP Id: rs1201215039
• gnomAD v3: 17-42571521-ATTTC-A
• gnomAD v4: 17-42571521-ATTTC-A
• MyVariant Identifiers: chr17:g.40723540_40723543del (hg19) ; chr17:g.42571522_42571525del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571524_42571527del , CM000679.2:g.42571524_42571527del	GRCh38
NC_000017.10:g.40723542_40723545del , CM000679.1:g.40723542_40723545del	GRCh37
NC_000017.9:g.37977068_37977071del	NCBI36
NG_029442.1:g.9465_9468del
NG_031960.1:g.11307_11310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.679-23_679-20del MANE Select	ENSP00000416627.1:n.679-23_679-20del
ENST00000246912.8:c.841-23_841-20del	ENSP00000246912.3:n.841-23_841-20del
ENST00000346833.8:c.589-23_589-20del	ENSP00000320913.3:n.589-23_589-20del
ENST00000435881.6:c.679-23_679-20del	ENSP00000416627.1:n.679-23_679-20del
ENST00000585403.5:n.886-23_886-20del
ENST00000588320.1:n.1155-23_1155-20del
ENST00000590050.5:n.845-23_845-20del
NM_170607.2:c.841-23_841-20del	NP_733752.1:n.841-23_841-20del
NM_198204.1:c.679-23_679-20del	NP_937847.1:n.679-23_679-20del
NM_198205.1:c.589-23_589-20del	NP_937848.1:n.589-23_589-20del
NM_198204.2:c.679-23_679-20del MANE Select	NP_937847.1:n.679-23_679-20del
NM_170607.3:c.841-23_841-20del	NP_733752.1:n.841-23_841-20del
NM_198205.2:c.589-23_589-20del	NP_937848.1:n.589-23_589-20del