Canonical Allele Identifier: CA2571859088

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571704_42571705del , CM000679.2:g.42571704_42571705del	GRCh38
NC_000017.10:g.40723722_40723723del , CM000679.1:g.40723722_40723723del	GRCh37
NC_000017.9:g.37977248_37977249del	NCBI36
NG_029442.1:g.9645_9646del
NG_031960.1:g.11130_11131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*101_*102del MANE Select	ENSP00000416627.1:n.*101_*102del
ENST00000246912.8:c.*101_*102del	ENSP00000246912.3:n.*101_*102del
ENST00000346833.8:c.*101_*102del	ENSP00000320913.3:n.*101_*102del
ENST00000435881.6:c.*101_*102del	ENSP00000416627.1:n.*101_*102del
ENST00000585403.5:n.1043_1044del
ENST00000588320.1:n.1312_1313del
ENST00000590050.5:n.1002_1003del
NM_170607.2:c.*101_*102del	NP_733752.1:n.*101_*102del
NM_198204.1:c.*101_*102del	NP_937847.1:n.*101_*102del
NM_198205.1:c.*101_*102del	NP_937848.1:n.*101_*102del
NM_198204.2:c.*101_*102del MANE Select	NP_937847.1:n.*101_*102del
NM_170607.3:c.*101_*102del	NP_733752.1:n.*101_*102del
NM_198205.2:c.*101_*102del	NP_937848.1:n.*101_*102del