Canonical Allele Identifier: CA500068439

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723588C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571570C>G , CM000679.2:g.42571570C>G	GRCh38
NC_000017.10:g.40723588C>G , CM000679.1:g.40723588C>G	GRCh37
NC_000017.9:g.37977114C>G	NCBI36
NG_029442.1:g.9511C>G
NG_031960.1:g.11262G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.702C>G MANE Select	ENSP00000416627.1:p.Gly234=
ENST00000246912.8:c.864C>G	ENSP00000246912.3:p.Gly288=
ENST00000346833.8:c.612C>G	ENSP00000320913.3:p.Gly204=
ENST00000435881.6:c.702C>G	ENSP00000416627.1:p.Gly234=
ENST00000585403.5:n.909C>G
ENST00000588320.1:n.1178C>G
ENST00000590050.5:n.868C>G
NM_170607.2:c.864C>G	NP_733752.1:p.Gly288=
NM_198204.1:c.702C>G	NP_937847.1:p.Gly234=
NM_198205.1:c.612C>G	NP_937848.1:p.Gly204=
NM_198204.2:c.702C>G MANE Select	NP_937847.1:p.Gly234=
NM_170607.3:c.864C>G	NP_733752.1:p.Gly288=
NM_198205.2:c.612C>G	NP_937848.1:p.Gly204=