Canonical Allele Identifier: CA290776502

Gene: MLX

Linked Data

• dbSNP Id: rs566859977
• gnomAD v3: 17-42571377-T-C
• gnomAD v4: 17-42571377-T-C
• MyVariant Identifiers: chr17:g.40723395T>C (hg19) ; chr17:g.42571377T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571377T>C , CM000679.2:g.42571377T>C	GRCh38
NC_000017.10:g.40723395T>C , CM000679.1:g.40723395T>C	GRCh37
NC_000017.9:g.37976921T>C	NCBI36
NG_029442.1:g.9318T>C
NG_031960.1:g.11455A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435881.7:c.679-170T>C MANE Select	ENSP00000416627.1:n.679-170T>C
ENST00000246912.8:c.841-170T>C	ENSP00000246912.3:n.841-170T>C
ENST00000346833.8:c.589-170T>C	ENSP00000320913.3:n.589-170T>C
ENST00000435881.6:c.679-170T>C	ENSP00000416627.1:n.679-170T>C
ENST00000585403.5:n.886-170T>C
ENST00000588320.1:n.1155-170T>C
ENST00000590050.5:n.845-170T>C
NM_170607.2:c.841-170T>C	NP_733752.1:n.841-170T>C
NM_198204.1:c.679-170T>C	NP_937847.1:n.679-170T>C
NM_198205.1:c.589-170T>C	NP_937848.1:n.589-170T>C
NM_198204.2:c.679-170T>C MANE Select	NP_937847.1:n.679-170T>C
NM_170607.3:c.841-170T>C	NP_733752.1:n.841-170T>C
NM_198205.2:c.589-170T>C	NP_937848.1:n.589-170T>C