Canonical Allele Identifier: CA2637983136

Gene: MLX

Linked Data

• gnomAD v4: 17-42571641-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571641C>G , CM000679.2:g.42571641C>G	GRCh38
NC_000017.10:g.40723659C>G , CM000679.1:g.40723659C>G	GRCh37
NC_000017.9:g.37977185C>G	NCBI36
NG_029442.1:g.9582C>G
NG_031960.1:g.11191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*38C>G MANE Select	ENSP00000416627.1:n.*38C>G
ENST00000246912.8:c.*38C>G	ENSP00000246912.3:n.*38C>G
ENST00000346833.8:c.*38C>G	ENSP00000320913.3:n.*38C>G
ENST00000435881.6:c.*38C>G	ENSP00000416627.1:n.*38C>G
ENST00000585403.5:n.980C>G
ENST00000588320.1:n.1249C>G
ENST00000590050.5:n.939C>G
NM_170607.2:c.*38C>G	NP_733752.1:n.*38C>G
NM_198204.1:c.*38C>G	NP_937847.1:n.*38C>G
NM_198205.1:c.*38C>G	NP_937848.1:n.*38C>G
NM_198204.2:c.*38C>G MANE Select	NP_937847.1:n.*38C>G
NM_170607.3:c.*38C>G	NP_733752.1:n.*38C>G
NM_198205.2:c.*38C>G	NP_937848.1:n.*38C>G