Canonical Allele Identifier: CA2637983034

Gene: MLX

Linked Data

• gnomAD v4: 17-42571399-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571399T>G , CM000679.2:g.42571399T>G	GRCh38
NC_000017.10:g.40723417T>G , CM000679.1:g.40723417T>G	GRCh37
NC_000017.9:g.37976943T>G	NCBI36
NG_029442.1:g.9340T>G
NG_031960.1:g.11433A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000435881.7:c.679-148T>G MANE Select	ENSP00000416627.1:n.679-148T>G
ENST00000246912.8:c.841-148T>G	ENSP00000246912.3:n.841-148T>G
ENST00000346833.8:c.589-148T>G	ENSP00000320913.3:n.589-148T>G
ENST00000435881.6:c.679-148T>G	ENSP00000416627.1:n.679-148T>G
ENST00000585403.5:n.886-148T>G
ENST00000588320.1:n.1155-148T>G
ENST00000590050.5:n.845-148T>G
NM_170607.2:c.841-148T>G	NP_733752.1:n.841-148T>G
NM_198204.1:c.679-148T>G	NP_937847.1:n.679-148T>G
NM_198205.1:c.589-148T>G	NP_937848.1:n.589-148T>G
NM_198204.2:c.679-148T>G MANE Select	NP_937847.1:n.679-148T>G
NM_170607.3:c.841-148T>G	NP_733752.1:n.841-148T>G
NM_198205.2:c.589-148T>G	NP_937848.1:n.589-148T>G