Canonical Allele Identifier: CA2403319468
Gene: HMGXB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267100_35267114delinsTTATATCTATCTGTA , CM000684.2:g.35267100_35267114delinsTTATATCTATCTGTA GRCh38
NC_000022.10:g.35663093_35663107delinsTTATATCTATCTGTA , CM000684.1:g.35663093_35663107delinsTTATATCTATCTGTA GRCh37
NC_000022.9:g.33993093_33993107delinsTTATATCTATCTGTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216106.6:c.1215+1497_1215+1511delinsTTATATCTATCTGTA MANE Select ENSP00000216106.5:n.1215+1497_1215+1511delinsTTATATCTATCTGTA
ENST00000216106.5:c.1215+1497_1215+1511delinsTTATATCTATCTGTA ENSP00000216106.5:n.1215+1497_1215+1511delinsTTATATCTATCTGTA
ENST00000418170.5:c.*1051+1497_*1051+1511delinsTTATATCTATCTGTA ENSP00000395532.1:n.*1051+1497_*1051+1511delinsTTATATCTATCTGT...
NM_001003681.2:c.1215+1497_1215+1511delinsTTATATCTATCTGTA NP_001003681.1:n.1215+1497_1215+1511delinsTTATATCTATCTGTA
NR_027780.1:n.1504+1497_1504+1511delinsTTATATCTATCTGTA
XM_006724100.2:c.1344+1497_1344+1511delinsTTATATCTATCTGTA XP_006724163.1:n.1344+1497_1344+1511delinsTTATATCTATCTGTA
XM_006724101.2:c.1344+1497_1344+1511delinsTTATATCTATCTGTA XP_006724164.1:n.1344+1497_1344+1511delinsTTATATCTATCTGTA
XM_006724102.1:c.888+1497_888+1511delinsTTATATCTATCTGTA XP_006724165.1:n.888+1497_888+1511delinsTTATATCTATCTGTA
XM_011529817.1:c.1215+1497_1215+1511delinsTTATATCTATCTGTA XP_011528119.1:n.1215+1497_1215+1511delinsTTATATCTATCTGTA
NM_001362972.1:c.888+1497_888+1511delinsTTATATCTATCTGTA NP_001349901.1:n.888+1497_888+1511delinsTTATATCTATCTGTA
XM_006724100.4:c.1344+1497_1344+1511delinsTTATATCTATCTGTA XP_006724163.1:n.1344+1497_1344+1511delinsTTATATCTATCTGTA
XM_006724101.4:c.1344+1497_1344+1511delinsTTATATCTATCTGTA XP_006724164.1:n.1344+1497_1344+1511delinsTTATATCTATCTGTA
XM_006724102.2:c.888+1497_888+1511delinsTTATATCTATCTGTA XP_006724165.1:n.888+1497_888+1511delinsTTATATCTATCTGTA
NM_001003681.3:c.1215+1497_1215+1511delinsTTATATCTATCTGTA MANE Select NP_001003681.1:n.1215+1497_1215+1511delinsTTATATCTATCTGTA
NM_001362972.2:c.888+1497_888+1511delinsTTATATCTATCTGTA NP_001349901.1:n.888+1497_888+1511delinsTTATATCTATCTGTA
NR_027780.2:n.1463+1497_1463+1511delinsTTATATCTATCTGTA