Canonical Allele Identifier: CA399605229

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723595C>A (hg19) ; chr17:g.42571577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571577C>A , CM000679.2:g.42571577C>A	GRCh38
NC_000017.10:g.40723595C>A , CM000679.1:g.40723595C>A	GRCh37
NC_000017.9:g.37977121C>A	NCBI36
NG_029442.1:g.9518C>A
NG_031960.1:g.11255G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.709C>A MANE Select	ENSP00000416627.1:p.His237Asn
ENST00000246912.8:c.871C>A	ENSP00000246912.3:p.His291Asn
ENST00000346833.8:c.619C>A	ENSP00000320913.3:p.His207Asn
ENST00000435881.6:c.709C>A	ENSP00000416627.1:p.His237Asn
ENST00000585403.5:n.916C>A
ENST00000588320.1:n.1185C>A
ENST00000590050.5:n.875C>A
NM_170607.2:c.871C>A	NP_733752.1:p.His291Asn
NM_198204.1:c.709C>A	NP_937847.1:p.His237Asn
NM_198205.1:c.619C>A	NP_937848.1:p.His207Asn
NM_198204.2:c.709C>A MANE Select	NP_937847.1:p.His237Asn
NM_170607.3:c.871C>A	NP_733752.1:p.His291Asn
NM_198205.2:c.619C>A	NP_937848.1:p.His207Asn