Canonical Allele Identifier: CA2403319551

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267174_35267176delinsTTA , CM000684.2:g.35267174_35267176delinsTTA	GRCh38
NC_000022.10:g.35663167_35663169delinsTTA , CM000684.1:g.35663167_35663169delinsTTA	GRCh37
NC_000022.9:g.33993167_33993169delinsTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1571_1215+1573delinsTTA MANE Select	ENSP00000216106.5:n.1215+1571_1215+1573delinsTTA
ENST00000216106.5:c.1215+1571_1215+1573delinsTTA	ENSP00000216106.5:n.1215+1571_1215+1573delinsTTA
ENST00000418170.5:c.*1051+1571_*1051+1573delinsTTA	ENSP00000395532.1:n.*1051+1571_*1051+1573delinsTTA
NM_001003681.2:c.1215+1571_1215+1573delinsTTA	NP_001003681.1:n.1215+1571_1215+1573delinsTTA
NR_027780.1:n.1504+1571_1504+1573delinsTTA
XM_006724100.2:c.1344+1571_1344+1573delinsTTA	XP_006724163.1:n.1344+1571_1344+1573delinsTTA
XM_006724101.2:c.1344+1571_1344+1573delinsTTA	XP_006724164.1:n.1344+1571_1344+1573delinsTTA
XM_006724102.1:c.888+1571_888+1573delinsTTA	XP_006724165.1:n.888+1571_888+1573delinsTTA
XM_011529817.1:c.1215+1571_1215+1573delinsTTA	XP_011528119.1:n.1215+1571_1215+1573delinsTTA
NM_001362972.1:c.888+1571_888+1573delinsTTA	NP_001349901.1:n.888+1571_888+1573delinsTTA
XM_006724100.4:c.1344+1571_1344+1573delinsTTA	XP_006724163.1:n.1344+1571_1344+1573delinsTTA
XM_006724101.4:c.1344+1571_1344+1573delinsTTA	XP_006724164.1:n.1344+1571_1344+1573delinsTTA
XM_006724102.2:c.888+1571_888+1573delinsTTA	XP_006724165.1:n.888+1571_888+1573delinsTTA
NM_001003681.3:c.1215+1571_1215+1573delinsTTA MANE Select	NP_001003681.1:n.1215+1571_1215+1573delinsTTA
NM_001362972.2:c.888+1571_888+1573delinsTTA	NP_001349901.1:n.888+1571_888+1573delinsTTA
NR_027780.2:n.1463+1571_1463+1573delinsTTA