Canonical Allele Identifier: CA2403319535

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267166_35267170delinsATAAT , CM000684.2:g.35267166_35267170delinsATAAT	GRCh38
NC_000022.10:g.35663159_35663163delinsATAAT , CM000684.1:g.35663159_35663163delinsATAAT	GRCh37
NC_000022.9:g.33993159_33993163delinsATAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1563_1215+1567delinsATAAT MANE Select	ENSP00000216106.5:n.1215+1563_1215+1567delinsATAAT
ENST00000216106.5:c.1215+1563_1215+1567delinsATAAT	ENSP00000216106.5:n.1215+1563_1215+1567delinsATAAT
ENST00000418170.5:c.*1051+1563_*1051+1567delinsATAAT	ENSP00000395532.1:n.*1051+1563_*1051+1567delinsATAAT
NM_001003681.2:c.1215+1563_1215+1567delinsATAAT	NP_001003681.1:n.1215+1563_1215+1567delinsATAAT
NR_027780.1:n.1504+1563_1504+1567delinsATAAT
XM_006724100.2:c.1344+1563_1344+1567delinsATAAT	XP_006724163.1:n.1344+1563_1344+1567delinsATAAT
XM_006724101.2:c.1344+1563_1344+1567delinsATAAT	XP_006724164.1:n.1344+1563_1344+1567delinsATAAT
XM_006724102.1:c.888+1563_888+1567delinsATAAT	XP_006724165.1:n.888+1563_888+1567delinsATAAT
XM_011529817.1:c.1215+1563_1215+1567delinsATAAT	XP_011528119.1:n.1215+1563_1215+1567delinsATAAT
NM_001362972.1:c.888+1563_888+1567delinsATAAT	NP_001349901.1:n.888+1563_888+1567delinsATAAT
XM_006724100.4:c.1344+1563_1344+1567delinsATAAT	XP_006724163.1:n.1344+1563_1344+1567delinsATAAT
XM_006724101.4:c.1344+1563_1344+1567delinsATAAT	XP_006724164.1:n.1344+1563_1344+1567delinsATAAT
XM_006724102.2:c.888+1563_888+1567delinsATAAT	XP_006724165.1:n.888+1563_888+1567delinsATAAT
NM_001003681.3:c.1215+1563_1215+1567delinsATAAT MANE Select	NP_001003681.1:n.1215+1563_1215+1567delinsATAAT
NM_001362972.2:c.888+1563_888+1567delinsATAAT	NP_001349901.1:n.888+1563_888+1567delinsATAAT
NR_027780.2:n.1463+1563_1463+1567delinsATAAT