Canonical Allele Identifier: CA772121403

Gene: MLX

Linked Data

• dbSNP Id: rs776226134
• MyVariant Identifiers: chr17:g.40723651A>T (hg19) ; chr17:g.42571633A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571633A>T , CM000679.2:g.42571633A>T	GRCh38
NC_000017.10:g.40723651A>T , CM000679.1:g.40723651A>T	GRCh37
NC_000017.9:g.37977177A>T	NCBI36
NG_029442.1:g.9574A>T
NG_031960.1:g.11199T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*30A>T MANE Select	ENSP00000416627.1:n.*30A>T
ENST00000246912.8:c.*30A>T	ENSP00000246912.3:n.*30A>T
ENST00000346833.8:c.*30A>T	ENSP00000320913.3:n.*30A>T
ENST00000435881.6:c.*30A>T	ENSP00000416627.1:n.*30A>T
ENST00000585403.5:n.972A>T
ENST00000588320.1:n.1241A>T
ENST00000590050.5:n.931A>T
NM_170607.2:c.*30A>T	NP_733752.1:n.*30A>T
NM_198204.1:c.*30A>T	NP_937847.1:n.*30A>T
NM_198205.1:c.*30A>T	NP_937848.1:n.*30A>T
NM_198204.2:c.*30A>T MANE Select	NP_937847.1:n.*30A>T
NM_170607.3:c.*30A>T	NP_733752.1:n.*30A>T
NM_198205.2:c.*30A>T	NP_937848.1:n.*30A>T