Canonical Allele Identifier: CA2733701980

Gene: MLX

Linked Data

• dbSNP Id: rs2143271423

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571622G>C , CM000679.2:g.42571622G>C	GRCh38
NC_000017.10:g.40723640G>C , CM000679.1:g.40723640G>C	GRCh37
NC_000017.9:g.37977166G>C	NCBI36
NG_029442.1:g.9563G>C
NG_031960.1:g.11210C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*19G>C MANE Select	ENSP00000416627.1:n.*19G>C
ENST00000246912.8:c.*19G>C	ENSP00000246912.3:n.*19G>C
ENST00000346833.8:c.*19G>C	ENSP00000320913.3:n.*19G>C
ENST00000435881.6:c.*19G>C	ENSP00000416627.1:n.*19G>C
ENST00000585403.5:n.961G>C
ENST00000588320.1:n.1230G>C
ENST00000590050.5:n.920G>C
NM_170607.2:c.*19G>C	NP_733752.1:n.*19G>C
NM_198204.1:c.*19G>C	NP_937847.1:n.*19G>C
NM_198205.1:c.*19G>C	NP_937848.1:n.*19G>C
NM_198204.2:c.*19G>C MANE Select	NP_937847.1:n.*19G>C
NM_170607.3:c.*19G>C	NP_733752.1:n.*19G>C
NM_198205.2:c.*19G>C	NP_937848.1:n.*19G>C