Canonical Allele Identifier: CA2637983032

Gene: MLX

Linked Data

• gnomAD v4: 17-42571398-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571398A>C , CM000679.2:g.42571398A>C	GRCh38
NC_000017.10:g.40723416A>C , CM000679.1:g.40723416A>C	GRCh37
NC_000017.9:g.37976942A>C	NCBI36
NG_029442.1:g.9339A>C
NG_031960.1:g.11434T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435881.7:c.679-149A>C MANE Select	ENSP00000416627.1:n.679-149A>C
ENST00000246912.8:c.841-149A>C	ENSP00000246912.3:n.841-149A>C
ENST00000346833.8:c.589-149A>C	ENSP00000320913.3:n.589-149A>C
ENST00000435881.6:c.679-149A>C	ENSP00000416627.1:n.679-149A>C
ENST00000585403.5:n.886-149A>C
ENST00000588320.1:n.1155-149A>C
ENST00000590050.5:n.845-149A>C
NM_170607.2:c.841-149A>C	NP_733752.1:n.841-149A>C
NM_198204.1:c.679-149A>C	NP_937847.1:n.679-149A>C
NM_198205.1:c.589-149A>C	NP_937848.1:n.589-149A>C
NM_198204.2:c.679-149A>C MANE Select	NP_937847.1:n.679-149A>C
NM_170607.3:c.841-149A>C	NP_733752.1:n.841-149A>C
NM_198205.2:c.589-149A>C	NP_937848.1:n.589-149A>C