Canonical Allele Identifier: CA1025386980

Gene: HMGXB4

Linked Data

• dbSNP Id: rs1923314380
• gnomAD v3: 22-35267168-A-AATAT
• gnomAD v4: 22-35267168-A-AATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267171_35267174dup , CM000684.2:g.35267171_35267174dup	GRCh38
NC_000022.10:g.35663164_35663167dup , CM000684.1:g.35663164_35663167dup	GRCh37
NC_000022.9:g.33993164_33993167dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1568_1215+1571dup MANE Select	ENSP00000216106.5:n.1215+1568_1215+1571dup
ENST00000216106.5:c.1215+1568_1215+1571dup	ENSP00000216106.5:n.1215+1568_1215+1571dup
ENST00000418170.5:c.*1051+1568_*1051+1571dup	ENSP00000395532.1:n.*1051+1568_*1051+1571dup
NM_001003681.2:c.1215+1568_1215+1571dup	NP_001003681.1:n.1215+1568_1215+1571dup
NR_027780.1:n.1504+1568_1504+1571dup
XM_006724100.2:c.1344+1568_1344+1571dup	XP_006724163.1:n.1344+1568_1344+1571dup
XM_006724101.2:c.1344+1568_1344+1571dup	XP_006724164.1:n.1344+1568_1344+1571dup
XM_006724102.1:c.888+1568_888+1571dup	XP_006724165.1:n.888+1568_888+1571dup
XM_011529817.1:c.1215+1568_1215+1571dup	XP_011528119.1:n.1215+1568_1215+1571dup
NM_001362972.1:c.888+1568_888+1571dup	NP_001349901.1:n.888+1568_888+1571dup
XM_006724100.4:c.1344+1568_1344+1571dup	XP_006724163.1:n.1344+1568_1344+1571dup
XM_006724101.4:c.1344+1568_1344+1571dup	XP_006724164.1:n.1344+1568_1344+1571dup
XM_006724102.2:c.888+1568_888+1571dup	XP_006724165.1:n.888+1568_888+1571dup
NM_001003681.3:c.1215+1568_1215+1571dup MANE Select	NP_001003681.1:n.1215+1568_1215+1571dup
NM_001362972.2:c.888+1568_888+1571dup	NP_001349901.1:n.888+1568_888+1571dup
NR_027780.2:n.1463+1568_1463+1571dup