Canonical Allele Identifier: CA2637983167

Gene: MLX

Linked Data

• gnomAD v4: 17-42571704-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571704A>C , CM000679.2:g.42571704A>C	GRCh38
NC_000017.10:g.40723722A>C , CM000679.1:g.40723722A>C	GRCh37
NC_000017.9:g.37977248A>C	NCBI36
NG_029442.1:g.9645A>C
NG_031960.1:g.11128T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*101A>C MANE Select	ENSP00000416627.1:n.*101A>C
ENST00000246912.8:c.*101A>C	ENSP00000246912.3:n.*101A>C
ENST00000346833.8:c.*101A>C	ENSP00000320913.3:n.*101A>C
ENST00000435881.6:c.*101A>C	ENSP00000416627.1:n.*101A>C
ENST00000585403.5:n.1043A>C
ENST00000588320.1:n.1312A>C
ENST00000590050.5:n.1002A>C
NM_170607.2:c.*101A>C	NP_733752.1:n.*101A>C
NM_198204.1:c.*101A>C	NP_937847.1:n.*101A>C
NM_198205.1:c.*101A>C	NP_937848.1:n.*101A>C
NM_198204.2:c.*101A>C MANE Select	NP_937847.1:n.*101A>C
NM_170607.3:c.*101A>C	NP_733752.1:n.*101A>C
NM_198205.2:c.*101A>C	NP_937848.1:n.*101A>C