Canonical Allele Identifier: CA399605326

Gene: MLX

Linked Data

• MyVariant Identifiers: chr17:g.40723612G>C (hg19) ; chr17:g.42571594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571594G>C , CM000679.2:g.42571594G>C	GRCh38
NC_000017.10:g.40723612G>C , CM000679.1:g.40723612G>C	GRCh37
NC_000017.9:g.37977138G>C	NCBI36
NG_029442.1:g.9535G>C
NG_031960.1:g.11238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.726G>C MANE Select	ENSP00000416627.1:p.Gln242His
ENST00000246912.8:c.888G>C	ENSP00000246912.3:p.Gln296His
ENST00000346833.8:c.636G>C	ENSP00000320913.3:p.Gln212His
ENST00000435881.6:c.726G>C	ENSP00000416627.1:p.Gln242His
ENST00000585403.5:n.933G>C
ENST00000588320.1:n.1202G>C
ENST00000590050.5:n.892G>C
NM_170607.2:c.888G>C	NP_733752.1:p.Gln296His
NM_198204.1:c.726G>C	NP_937847.1:p.Gln242His
NM_198205.1:c.636G>C	NP_937848.1:p.Gln212His
NM_198204.2:c.726G>C MANE Select	NP_937847.1:p.Gln242His
NM_170607.3:c.888G>C	NP_733752.1:p.Gln296His
NM_198205.2:c.636G>C	NP_937848.1:p.Gln212His