Canonical Allele Identifier: CA2637983164

Gene: MLX

Linked Data

• gnomAD v4: 17-42571698-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571700_42571701del , CM000679.2:g.42571700_42571701del	GRCh38
NC_000017.10:g.40723718_40723719del , CM000679.1:g.40723718_40723719del	GRCh37
NC_000017.9:g.37977244_37977245del	NCBI36
NG_029442.1:g.9641_9642del
NG_031960.1:g.11132_11133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*97_*98del MANE Select	ENSP00000416627.1:n.*97_*98del
ENST00000246912.8:c.*97_*98del	ENSP00000246912.3:n.*97_*98del
ENST00000346833.8:c.*97_*98del	ENSP00000320913.3:n.*97_*98del
ENST00000435881.6:c.*97_*98del	ENSP00000416627.1:n.*97_*98del
ENST00000585403.5:n.1039_1040del
ENST00000588320.1:n.1308_1309del
ENST00000590050.5:n.998_999del
NM_170607.2:c.*97_*98del	NP_733752.1:n.*97_*98del
NM_198204.1:c.*97_*98del	NP_937847.1:n.*97_*98del
NM_198205.1:c.*97_*98del	NP_937848.1:n.*97_*98del
NM_198204.2:c.*97_*98del MANE Select	NP_937847.1:n.*97_*98del
NM_170607.3:c.*97_*98del	NP_733752.1:n.*97_*98del
NM_198205.2:c.*97_*98del	NP_937848.1:n.*97_*98del