Canonical Allele Identifier: CA1025386863
Gene: HMGXB4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.35267146_35267147del , CM000684.2:g.35267146_35267147del GRCh38
NC_000022.10:g.35663139_35663140del , CM000684.1:g.35663139_35663140del GRCh37
NC_000022.9:g.33993139_33993140del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216106.6:c.1215+1543_1215+1544del MANE Select ENSP00000216106.5:n.1215+1543_1215+1544del
ENST00000216106.5:c.1215+1543_1215+1544del ENSP00000216106.5:n.1215+1543_1215+1544del
ENST00000418170.5:c.*1051+1543_*1051+1544del ENSP00000395532.1:n.*1051+1543_*1051+1544del
NM_001003681.2:c.1215+1543_1215+1544del NP_001003681.1:n.1215+1543_1215+1544del
NR_027780.1:n.1504+1543_1504+1544del
XM_006724100.2:c.1344+1543_1344+1544del XP_006724163.1:n.1344+1543_1344+1544del
XM_006724101.2:c.1344+1543_1344+1544del XP_006724164.1:n.1344+1543_1344+1544del
XM_006724102.1:c.888+1543_888+1544del XP_006724165.1:n.888+1543_888+1544del
XM_011529817.1:c.1215+1543_1215+1544del XP_011528119.1:n.1215+1543_1215+1544del
NM_001362972.1:c.888+1543_888+1544del NP_001349901.1:n.888+1543_888+1544del
XM_006724100.4:c.1344+1543_1344+1544del XP_006724163.1:n.1344+1543_1344+1544del
XM_006724101.4:c.1344+1543_1344+1544del XP_006724164.1:n.1344+1543_1344+1544del
XM_006724102.2:c.888+1543_888+1544del XP_006724165.1:n.888+1543_888+1544del
NM_001003681.3:c.1215+1543_1215+1544del MANE Select NP_001003681.1:n.1215+1543_1215+1544del
NM_001362972.2:c.888+1543_888+1544del NP_001349901.1:n.888+1543_888+1544del
NR_027780.2:n.1463+1543_1463+1544del