Canonical Allele Identifier: CA2637983151

Gene: MLX

Linked Data

• gnomAD v4: 17-42571671-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571671C>A , CM000679.2:g.42571671C>A	GRCh38
NC_000017.10:g.40723689C>A , CM000679.1:g.40723689C>A	GRCh37
NC_000017.9:g.37977215C>A	NCBI36
NG_029442.1:g.9612C>A
NG_031960.1:g.11161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*68C>A MANE Select	ENSP00000416627.1:n.*68C>A
ENST00000246912.8:c.*68C>A	ENSP00000246912.3:n.*68C>A
ENST00000346833.8:c.*68C>A	ENSP00000320913.3:n.*68C>A
ENST00000435881.6:c.*68C>A	ENSP00000416627.1:n.*68C>A
ENST00000585403.5:n.1010C>A
ENST00000588320.1:n.1279C>A
ENST00000590050.5:n.969C>A
NM_170607.2:c.*68C>A	NP_733752.1:n.*68C>A
NM_198204.1:c.*68C>A	NP_937847.1:n.*68C>A
NM_198205.1:c.*68C>A	NP_937848.1:n.*68C>A
NM_198204.2:c.*68C>A MANE Select	NP_937847.1:n.*68C>A
NM_170607.3:c.*68C>A	NP_733752.1:n.*68C>A
NM_198205.2:c.*68C>A	NP_937848.1:n.*68C>A