Canonical Allele Identifier: CA2637983190

Gene: MLX

Linked Data

• gnomAD v4: 17-42571737-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571737T>C , CM000679.2:g.42571737T>C	GRCh38
NC_000017.10:g.40723755T>C , CM000679.1:g.40723755T>C	GRCh37
NC_000017.9:g.37977281T>C	NCBI36
NG_029442.1:g.9678T>C
NG_031960.1:g.11095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*134T>C MANE Select	ENSP00000416627.1:n.*134T>C
ENST00000246912.8:c.*134T>C	ENSP00000246912.3:n.*134T>C
ENST00000346833.8:c.*134T>C	ENSP00000320913.3:n.*134T>C
ENST00000435881.6:c.*134T>C	ENSP00000416627.1:n.*134T>C
ENST00000588320.1:n.1345T>C
ENST00000590050.5:n.1035T>C
NM_170607.2:c.*134T>C	NP_733752.1:n.*134T>C
NM_198204.1:c.*134T>C	NP_937847.1:n.*134T>C
NM_198205.1:c.*134T>C	NP_937848.1:n.*134T>C
NM_198204.2:c.*134T>C MANE Select	NP_937847.1:n.*134T>C
NM_170607.3:c.*134T>C	NP_733752.1:n.*134T>C
NM_198205.2:c.*134T>C	NP_937848.1:n.*134T>C