Canonical Allele Identifier: CA2533340992

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571521_42571524del , CM000679.2:g.42571521_42571524del	GRCh38
NC_000017.10:g.40723539_40723542del , CM000679.1:g.40723539_40723542del	GRCh37
NC_000017.9:g.37977065_37977068del	NCBI36
NG_029442.1:g.9462_9465del
NG_031960.1:g.11309_11312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.679-26_679-23del MANE Select	ENSP00000416627.1:n.679-26_679-23del
ENST00000246912.8:c.841-26_841-23del	ENSP00000246912.3:n.841-26_841-23del
ENST00000346833.8:c.589-26_589-23del	ENSP00000320913.3:n.589-26_589-23del
ENST00000435881.6:c.679-26_679-23del	ENSP00000416627.1:n.679-26_679-23del
ENST00000585403.5:n.886-26_886-23del
ENST00000588320.1:n.1155-26_1155-23del
ENST00000590050.5:n.845-26_845-23del
NM_170607.2:c.841-26_841-23del	NP_733752.1:n.841-26_841-23del
NM_198204.1:c.679-26_679-23del	NP_937847.1:n.679-26_679-23del
NM_198205.1:c.589-26_589-23del	NP_937848.1:n.589-26_589-23del
NM_198204.2:c.679-26_679-23del MANE Select	NP_937847.1:n.679-26_679-23del
NM_170607.3:c.841-26_841-23del	NP_733752.1:n.841-26_841-23del
NM_198205.2:c.589-26_589-23del	NP_937848.1:n.589-26_589-23del