Canonical Allele Identifier: CA2637983170

Gene: MLX

Linked Data

• gnomAD v4: 17-42571706-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571706T>C , CM000679.2:g.42571706T>C	GRCh38
NC_000017.10:g.40723724T>C , CM000679.1:g.40723724T>C	GRCh37
NC_000017.9:g.37977250T>C	NCBI36
NG_029442.1:g.9647T>C
NG_031960.1:g.11126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*103T>C MANE Select	ENSP00000416627.1:n.*103T>C
ENST00000246912.8:c.*103T>C	ENSP00000246912.3:n.*103T>C
ENST00000346833.8:c.*103T>C	ENSP00000320913.3:n.*103T>C
ENST00000435881.6:c.*103T>C	ENSP00000416627.1:n.*103T>C
ENST00000585403.5:n.1045T>C
ENST00000588320.1:n.1314T>C
ENST00000590050.5:n.1004T>C
NM_170607.2:c.*103T>C	NP_733752.1:n.*103T>C
NM_198204.1:c.*103T>C	NP_937847.1:n.*103T>C
NM_198205.1:c.*103T>C	NP_937848.1:n.*103T>C
NM_198204.2:c.*103T>C MANE Select	NP_937847.1:n.*103T>C
NM_170607.3:c.*103T>C	NP_733752.1:n.*103T>C
NM_198205.2:c.*103T>C	NP_937848.1:n.*103T>C