Canonical Allele Identifier: CA626054617

Gene: MLX

Linked Data

• dbSNP Id: rs772457859
• gnomAD v2: 17-40723624-G-T
• gnomAD v4: 17-42571606-G-T
• MyVariant Identifiers: chr17:g.40723624G>T (hg19) ; chr17:g.42571606G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571606G>T , CM000679.2:g.42571606G>T	GRCh38
NC_000017.10:g.40723624G>T , CM000679.1:g.40723624G>T	GRCh37
NC_000017.9:g.37977150G>T	NCBI36
NG_029442.1:g.9547G>T
NG_031960.1:g.11226C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*3G>T MANE Select	ENSP00000416627.1:n.*3G>T
ENST00000246912.8:c.*3G>T	ENSP00000246912.3:n.*3G>T
ENST00000346833.8:c.*3G>T	ENSP00000320913.3:n.*3G>T
ENST00000435881.6:c.*3G>T	ENSP00000416627.1:n.*3G>T
ENST00000585403.5:n.945G>T
ENST00000588320.1:n.1214G>T
ENST00000590050.5:n.904G>T
NM_170607.2:c.*3G>T	NP_733752.1:n.*3G>T
NM_198204.1:c.*3G>T	NP_937847.1:n.*3G>T
NM_198205.1:c.*3G>T	NP_937848.1:n.*3G>T
NM_198204.2:c.*3G>T MANE Select	NP_937847.1:n.*3G>T
NM_170607.3:c.*3G>T	NP_733752.1:n.*3G>T
NM_198205.2:c.*3G>T	NP_937848.1:n.*3G>T