Canonical Allele Identifier: CA500068450

Gene: MLX

Linked Data

• dbSNP Id: rs2093032920
• MyVariant Identifiers: chr17:g.40723592C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571574C>T , CM000679.2:g.42571574C>T	GRCh38
NC_000017.10:g.40723592C>T , CM000679.1:g.40723592C>T	GRCh37
NC_000017.9:g.37977118C>T	NCBI36
NG_029442.1:g.9515C>T
NG_031960.1:g.11258G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.706C>T MANE Select	ENSP00000416627.1:p.Leu236=
ENST00000246912.8:c.868C>T	ENSP00000246912.3:p.Leu290=
ENST00000346833.8:c.616C>T	ENSP00000320913.3:p.Leu206=
ENST00000435881.6:c.706C>T	ENSP00000416627.1:p.Leu236=
ENST00000585403.5:n.913C>T
ENST00000588320.1:n.1182C>T
ENST00000590050.5:n.872C>T
NM_170607.2:c.868C>T	NP_733752.1:p.Leu290=
NM_198204.1:c.706C>T	NP_937847.1:p.Leu236=
NM_198205.1:c.616C>T	NP_937848.1:p.Leu206=
NM_198204.2:c.706C>T MANE Select	NP_937847.1:p.Leu236=
NM_170607.3:c.868C>T	NP_733752.1:p.Leu290=
NM_198205.2:c.616C>T	NP_937848.1:p.Leu206=