Canonical Allele Identifier: CA772121187

Gene: MLX

Linked Data

• dbSNP Id: rs1421458526
• MyVariant Identifiers: chr17:g.40723416A>T (hg19) ; chr17:g.42571398A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571398A>T , CM000679.2:g.42571398A>T	GRCh38
NC_000017.10:g.40723416A>T , CM000679.1:g.40723416A>T	GRCh37
NC_000017.9:g.37976942A>T	NCBI36
NG_029442.1:g.9339A>T
NG_031960.1:g.11434T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000435881.7:c.679-149A>T MANE Select	ENSP00000416627.1:n.679-149A>T
ENST00000246912.8:c.841-149A>T	ENSP00000246912.3:n.841-149A>T
ENST00000346833.8:c.589-149A>T	ENSP00000320913.3:n.589-149A>T
ENST00000435881.6:c.679-149A>T	ENSP00000416627.1:n.679-149A>T
ENST00000585403.5:n.886-149A>T
ENST00000588320.1:n.1155-149A>T
ENST00000590050.5:n.845-149A>T
NM_170607.2:c.841-149A>T	NP_733752.1:n.841-149A>T
NM_198204.1:c.679-149A>T	NP_937847.1:n.679-149A>T
NM_198205.1:c.589-149A>T	NP_937848.1:n.589-149A>T
NM_198204.2:c.679-149A>T MANE Select	NP_937847.1:n.679-149A>T
NM_170607.3:c.841-149A>T	NP_733752.1:n.841-149A>T
NM_198205.2:c.589-149A>T	NP_937848.1:n.589-149A>T