Canonical Allele Identifier: CA399605243

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723597C>A (hg19) ; chr17:g.42571579C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571579C>A , CM000679.2:g.42571579C>A	GRCh38
NC_000017.10:g.40723597C>A , CM000679.1:g.40723597C>A	GRCh37
NC_000017.9:g.37977123C>A	NCBI36
NG_029442.1:g.9520C>A
NG_031960.1:g.11253G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.711C>A MANE Select	ENSP00000416627.1:p.His237Gln
ENST00000246912.8:c.873C>A	ENSP00000246912.3:p.His291Gln
ENST00000346833.8:c.621C>A	ENSP00000320913.3:p.His207Gln
ENST00000435881.6:c.711C>A	ENSP00000416627.1:p.His237Gln
ENST00000585403.5:n.918C>A
ENST00000588320.1:n.1187C>A
ENST00000590050.5:n.877C>A
NM_170607.2:c.873C>A	NP_733752.1:p.His291Gln
NM_198204.1:c.711C>A	NP_937847.1:p.His237Gln
NM_198205.1:c.621C>A	NP_937848.1:p.His207Gln
NM_198204.2:c.711C>A MANE Select	NP_937847.1:p.His237Gln
NM_170607.3:c.873C>A	NP_733752.1:p.His291Gln
NM_198205.2:c.621C>A	NP_937848.1:p.His207Gln