Canonical Allele Identifier: CA2403319482

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267124_35267128delinsCTGTT , CM000684.2:g.35267124_35267128delinsCTGTT	GRCh38
NC_000022.10:g.35663117_35663121delinsCTGTT , CM000684.1:g.35663117_35663121delinsCTGTT	GRCh37
NC_000022.9:g.33993117_33993121delinsCTGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1521_1215+1525delinsCTGTT MANE Select	ENSP00000216106.5:n.1215+1521_1215+1525delinsCTGTT
ENST00000216106.5:c.1215+1521_1215+1525delinsCTGTT	ENSP00000216106.5:n.1215+1521_1215+1525delinsCTGTT
ENST00000418170.5:c.*1051+1521_*1051+1525delinsCTGTT	ENSP00000395532.1:n.*1051+1521_*1051+1525delinsCTGTT
NM_001003681.2:c.1215+1521_1215+1525delinsCTGTT	NP_001003681.1:n.1215+1521_1215+1525delinsCTGTT
NR_027780.1:n.1504+1521_1504+1525delinsCTGTT
XM_006724100.2:c.1344+1521_1344+1525delinsCTGTT	XP_006724163.1:n.1344+1521_1344+1525delinsCTGTT
XM_006724101.2:c.1344+1521_1344+1525delinsCTGTT	XP_006724164.1:n.1344+1521_1344+1525delinsCTGTT
XM_006724102.1:c.888+1521_888+1525delinsCTGTT	XP_006724165.1:n.888+1521_888+1525delinsCTGTT
XM_011529817.1:c.1215+1521_1215+1525delinsCTGTT	XP_011528119.1:n.1215+1521_1215+1525delinsCTGTT
NM_001362972.1:c.888+1521_888+1525delinsCTGTT	NP_001349901.1:n.888+1521_888+1525delinsCTGTT
XM_006724100.4:c.1344+1521_1344+1525delinsCTGTT	XP_006724163.1:n.1344+1521_1344+1525delinsCTGTT
XM_006724101.4:c.1344+1521_1344+1525delinsCTGTT	XP_006724164.1:n.1344+1521_1344+1525delinsCTGTT
XM_006724102.2:c.888+1521_888+1525delinsCTGTT	XP_006724165.1:n.888+1521_888+1525delinsCTGTT
NM_001003681.3:c.1215+1521_1215+1525delinsCTGTT MANE Select	NP_001003681.1:n.1215+1521_1215+1525delinsCTGTT
NM_001362972.2:c.888+1521_888+1525delinsCTGTT	NP_001349901.1:n.888+1521_888+1525delinsCTGTT
NR_027780.2:n.1463+1521_1463+1525delinsCTGTT