Canonical Allele Identifier: CA2403319462

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267099_35267103delinsTTTAT , CM000684.2:g.35267099_35267103delinsTTTAT	GRCh38
NC_000022.10:g.35663092_35663096delinsTTTAT , CM000684.1:g.35663092_35663096delinsTTTAT	GRCh37
NC_000022.9:g.33993092_33993096delinsTTTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1496_1215+1500delinsTTTAT MANE Select	ENSP00000216106.5:n.1215+1496_1215+1500delinsTTTAT
ENST00000216106.5:c.1215+1496_1215+1500delinsTTTAT	ENSP00000216106.5:n.1215+1496_1215+1500delinsTTTAT
ENST00000418170.5:c.*1051+1496_*1051+1500delinsTTTAT	ENSP00000395532.1:n.*1051+1496_*1051+1500delinsTTTAT
NM_001003681.2:c.1215+1496_1215+1500delinsTTTAT	NP_001003681.1:n.1215+1496_1215+1500delinsTTTAT
NR_027780.1:n.1504+1496_1504+1500delinsTTTAT
XM_006724100.2:c.1344+1496_1344+1500delinsTTTAT	XP_006724163.1:n.1344+1496_1344+1500delinsTTTAT
XM_006724101.2:c.1344+1496_1344+1500delinsTTTAT	XP_006724164.1:n.1344+1496_1344+1500delinsTTTAT
XM_006724102.1:c.888+1496_888+1500delinsTTTAT	XP_006724165.1:n.888+1496_888+1500delinsTTTAT
XM_011529817.1:c.1215+1496_1215+1500delinsTTTAT	XP_011528119.1:n.1215+1496_1215+1500delinsTTTAT
NM_001362972.1:c.888+1496_888+1500delinsTTTAT	NP_001349901.1:n.888+1496_888+1500delinsTTTAT
XM_006724100.4:c.1344+1496_1344+1500delinsTTTAT	XP_006724163.1:n.1344+1496_1344+1500delinsTTTAT
XM_006724101.4:c.1344+1496_1344+1500delinsTTTAT	XP_006724164.1:n.1344+1496_1344+1500delinsTTTAT
XM_006724102.2:c.888+1496_888+1500delinsTTTAT	XP_006724165.1:n.888+1496_888+1500delinsTTTAT
NM_001003681.3:c.1215+1496_1215+1500delinsTTTAT MANE Select	NP_001003681.1:n.1215+1496_1215+1500delinsTTTAT
NM_001362972.2:c.888+1496_888+1500delinsTTTAT	NP_001349901.1:n.888+1496_888+1500delinsTTTAT
NR_027780.2:n.1463+1496_1463+1500delinsTTTAT