Canonical Allele Identifier: CA2260544172

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571582_42571583delinsAT , CM000679.2:g.42571582_42571583delinsAT	GRCh38
NC_000017.10:g.40723600_40723601delinsAT , CM000679.1:g.40723600_40723601delinsAT	GRCh37
NC_000017.9:g.37977126_37977127delinsAT	NCBI36
NG_029442.1:g.9523_9524delinsAT
NG_031960.1:g.11249_11250delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.714_715delinsAT MANE Select	ENSP00000416627.1:p.Gln238=
ENST00000246912.8:c.876_877delinsAT	ENSP00000246912.3:p.Gln292=
ENST00000346833.8:c.624_625delinsAT	ENSP00000320913.3:p.Gln208=
ENST00000435881.6:c.714_715delinsAT	ENSP00000416627.1:p.Gln238=
ENST00000585403.5:n.921_922delinsAT
ENST00000588320.1:n.1190_1191delinsAT
ENST00000590050.5:n.880_881delinsAT
NM_170607.2:c.876_877delinsAT	NP_733752.1:p.Gln292=
NM_198204.1:c.714_715delinsAT	NP_937847.1:p.Gln238=
NM_198205.1:c.624_625delinsAT	NP_937848.1:p.Gln208=
NM_198204.2:c.714_715delinsAT MANE Select	NP_937847.1:p.Gln238=
NM_170607.3:c.876_877delinsAT	NP_733752.1:p.Gln292=
NM_198205.2:c.624_625delinsAT	NP_937848.1:p.Gln208=