Canonical Allele Identifier: CA2403319449
Gene: HMGXB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267085_35267099delinsCTTATATCTATCTGT , CM000684.2:g.35267085_35267099delinsCTTATATCTATCTGT GRCh38
NC_000022.10:g.35663078_35663092delinsCTTATATCTATCTGT , CM000684.1:g.35663078_35663092delinsCTTATATCTATCTGT GRCh37
NC_000022.9:g.33993078_33993092delinsCTTATATCTATCTGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216106.6:c.1215+1482_1215+1496delinsCTTATATCTATCTGT MANE Select ENSP00000216106.5:n.1215+1482_1215+1496delinsCTTATATCTATCTGT
ENST00000216106.5:c.1215+1482_1215+1496delinsCTTATATCTATCTGT ENSP00000216106.5:n.1215+1482_1215+1496delinsCTTATATCTATCTGT
ENST00000418170.5:c.*1051+1482_*1051+1496delinsCTTATATCTATCTGT ENSP00000395532.1:n.*1051+1482_*1051+1496delinsCTTATATCTATCTG...
NM_001003681.2:c.1215+1482_1215+1496delinsCTTATATCTATCTGT NP_001003681.1:n.1215+1482_1215+1496delinsCTTATATCTATCTGT
NR_027780.1:n.1504+1482_1504+1496delinsCTTATATCTATCTGT
XM_006724100.2:c.1344+1482_1344+1496delinsCTTATATCTATCTGT XP_006724163.1:n.1344+1482_1344+1496delinsCTTATATCTATCTGT
XM_006724101.2:c.1344+1482_1344+1496delinsCTTATATCTATCTGT XP_006724164.1:n.1344+1482_1344+1496delinsCTTATATCTATCTGT
XM_006724102.1:c.888+1482_888+1496delinsCTTATATCTATCTGT XP_006724165.1:n.888+1482_888+1496delinsCTTATATCTATCTGT
XM_011529817.1:c.1215+1482_1215+1496delinsCTTATATCTATCTGT XP_011528119.1:n.1215+1482_1215+1496delinsCTTATATCTATCTGT
NM_001362972.1:c.888+1482_888+1496delinsCTTATATCTATCTGT NP_001349901.1:n.888+1482_888+1496delinsCTTATATCTATCTGT
XM_006724100.4:c.1344+1482_1344+1496delinsCTTATATCTATCTGT XP_006724163.1:n.1344+1482_1344+1496delinsCTTATATCTATCTGT
XM_006724101.4:c.1344+1482_1344+1496delinsCTTATATCTATCTGT XP_006724164.1:n.1344+1482_1344+1496delinsCTTATATCTATCTGT
XM_006724102.2:c.888+1482_888+1496delinsCTTATATCTATCTGT XP_006724165.1:n.888+1482_888+1496delinsCTTATATCTATCTGT
NM_001003681.3:c.1215+1482_1215+1496delinsCTTATATCTATCTGT MANE Select NP_001003681.1:n.1215+1482_1215+1496delinsCTTATATCTATCTGT
NM_001362972.2:c.888+1482_888+1496delinsCTTATATCTATCTGT NP_001349901.1:n.888+1482_888+1496delinsCTTATATCTATCTGT
NR_027780.2:n.1463+1482_1463+1496delinsCTTATATCTATCTGT