Canonical Allele Identifier: CA2403319499

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267145_35267146delinsTG , CM000684.2:g.35267145_35267146delinsTG	GRCh38
NC_000022.10:g.35663138_35663139delinsTG , CM000684.1:g.35663138_35663139delinsTG	GRCh37
NC_000022.9:g.33993138_33993139delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1542_1215+1543delinsTG MANE Select	ENSP00000216106.5:n.1215+1542_1215+1543delinsTG
ENST00000216106.5:c.1215+1542_1215+1543delinsTG	ENSP00000216106.5:n.1215+1542_1215+1543delinsTG
ENST00000418170.5:c.*1051+1542_*1051+1543delinsTG	ENSP00000395532.1:n.*1051+1542_*1051+1543delinsTG
NM_001003681.2:c.1215+1542_1215+1543delinsTG	NP_001003681.1:n.1215+1542_1215+1543delinsTG
NR_027780.1:n.1504+1542_1504+1543delinsTG
XM_006724100.2:c.1344+1542_1344+1543delinsTG	XP_006724163.1:n.1344+1542_1344+1543delinsTG
XM_006724101.2:c.1344+1542_1344+1543delinsTG	XP_006724164.1:n.1344+1542_1344+1543delinsTG
XM_006724102.1:c.888+1542_888+1543delinsTG	XP_006724165.1:n.888+1542_888+1543delinsTG
XM_011529817.1:c.1215+1542_1215+1543delinsTG	XP_011528119.1:n.1215+1542_1215+1543delinsTG
NM_001362972.1:c.888+1542_888+1543delinsTG	NP_001349901.1:n.888+1542_888+1543delinsTG
XM_006724100.4:c.1344+1542_1344+1543delinsTG	XP_006724163.1:n.1344+1542_1344+1543delinsTG
XM_006724101.4:c.1344+1542_1344+1543delinsTG	XP_006724164.1:n.1344+1542_1344+1543delinsTG
XM_006724102.2:c.888+1542_888+1543delinsTG	XP_006724165.1:n.888+1542_888+1543delinsTG
NM_001003681.3:c.1215+1542_1215+1543delinsTG MANE Select	NP_001003681.1:n.1215+1542_1215+1543delinsTG
NM_001362972.2:c.888+1542_888+1543delinsTG	NP_001349901.1:n.888+1542_888+1543delinsTG
NR_027780.2:n.1463+1542_1463+1543delinsTG