Canonical Allele Identifier: CA2403319528

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267162_35267166delinsTAAAA , CM000684.2:g.35267162_35267166delinsTAAAA	GRCh38
NC_000022.10:g.35663155_35663159delinsTAAAA , CM000684.1:g.35663155_35663159delinsTAAAA	GRCh37
NC_000022.9:g.33993155_33993159delinsTAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1559_1215+1563delinsTAAAA MANE Select	ENSP00000216106.5:n.1215+1559_1215+1563delinsTAAAA
ENST00000216106.5:c.1215+1559_1215+1563delinsTAAAA	ENSP00000216106.5:n.1215+1559_1215+1563delinsTAAAA
ENST00000418170.5:c.*1051+1559_*1051+1563delinsTAAAA	ENSP00000395532.1:n.*1051+1559_*1051+1563delinsTAAAA
NM_001003681.2:c.1215+1559_1215+1563delinsTAAAA	NP_001003681.1:n.1215+1559_1215+1563delinsTAAAA
NR_027780.1:n.1504+1559_1504+1563delinsTAAAA
XM_006724100.2:c.1344+1559_1344+1563delinsTAAAA	XP_006724163.1:n.1344+1559_1344+1563delinsTAAAA
XM_006724101.2:c.1344+1559_1344+1563delinsTAAAA	XP_006724164.1:n.1344+1559_1344+1563delinsTAAAA
XM_006724102.1:c.888+1559_888+1563delinsTAAAA	XP_006724165.1:n.888+1559_888+1563delinsTAAAA
XM_011529817.1:c.1215+1559_1215+1563delinsTAAAA	XP_011528119.1:n.1215+1559_1215+1563delinsTAAAA
NM_001362972.1:c.888+1559_888+1563delinsTAAAA	NP_001349901.1:n.888+1559_888+1563delinsTAAAA
XM_006724100.4:c.1344+1559_1344+1563delinsTAAAA	XP_006724163.1:n.1344+1559_1344+1563delinsTAAAA
XM_006724101.4:c.1344+1559_1344+1563delinsTAAAA	XP_006724164.1:n.1344+1559_1344+1563delinsTAAAA
XM_006724102.2:c.888+1559_888+1563delinsTAAAA	XP_006724165.1:n.888+1559_888+1563delinsTAAAA
NM_001003681.3:c.1215+1559_1215+1563delinsTAAAA MANE Select	NP_001003681.1:n.1215+1559_1215+1563delinsTAAAA
NM_001362972.2:c.888+1559_888+1563delinsTAAAA	NP_001349901.1:n.888+1559_888+1563delinsTAAAA
NR_027780.2:n.1463+1559_1463+1563delinsTAAAA