Canonical Allele Identifier: CA399605314

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723610C>T (hg19) ; chr17:g.42571592C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571592C>T , CM000679.2:g.42571592C>T	GRCh38
NC_000017.10:g.40723610C>T , CM000679.1:g.40723610C>T	GRCh37
NC_000017.9:g.37977136C>T	NCBI36
NG_029442.1:g.9533C>T
NG_031960.1:g.11240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.724C>T MANE Select	ENSP00000416627.1:p.Gln242Ter
ENST00000246912.8:c.886C>T	ENSP00000246912.3:p.Gln296Ter
ENST00000346833.8:c.634C>T	ENSP00000320913.3:p.Gln212Ter
ENST00000435881.6:c.724C>T	ENSP00000416627.1:p.Gln242Ter
ENST00000585403.5:n.931C>T
ENST00000588320.1:n.1200C>T
ENST00000590050.5:n.890C>T
NM_170607.2:c.886C>T	NP_733752.1:p.Gln296Ter
NM_198204.1:c.724C>T	NP_937847.1:p.Gln242Ter
NM_198205.1:c.634C>T	NP_937848.1:p.Gln212Ter
NM_198204.2:c.724C>T MANE Select	NP_937847.1:p.Gln242Ter
NM_170607.3:c.886C>T	NP_733752.1:p.Gln296Ter
NM_198205.2:c.634C>T	NP_937848.1:p.Gln212Ter