Canonical Allele Identifier: CA2403319546

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267173_35267174delinsAT , CM000684.2:g.35267173_35267174delinsAT	GRCh38
NC_000022.10:g.35663166_35663167delinsAT , CM000684.1:g.35663166_35663167delinsAT	GRCh37
NC_000022.9:g.33993166_33993167delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1570_1215+1571delinsAT MANE Select	ENSP00000216106.5:n.1215+1570_1215+1571delinsAT
ENST00000216106.5:c.1215+1570_1215+1571delinsAT	ENSP00000216106.5:n.1215+1570_1215+1571delinsAT
ENST00000418170.5:c.*1051+1570_*1051+1571delinsAT	ENSP00000395532.1:n.*1051+1570_*1051+1571delinsAT
NM_001003681.2:c.1215+1570_1215+1571delinsAT	NP_001003681.1:n.1215+1570_1215+1571delinsAT
NR_027780.1:n.1504+1570_1504+1571delinsAT
XM_006724100.2:c.1344+1570_1344+1571delinsAT	XP_006724163.1:n.1344+1570_1344+1571delinsAT
XM_006724101.2:c.1344+1570_1344+1571delinsAT	XP_006724164.1:n.1344+1570_1344+1571delinsAT
XM_006724102.1:c.888+1570_888+1571delinsAT	XP_006724165.1:n.888+1570_888+1571delinsAT
XM_011529817.1:c.1215+1570_1215+1571delinsAT	XP_011528119.1:n.1215+1570_1215+1571delinsAT
NM_001362972.1:c.888+1570_888+1571delinsAT	NP_001349901.1:n.888+1570_888+1571delinsAT
XM_006724100.4:c.1344+1570_1344+1571delinsAT	XP_006724163.1:n.1344+1570_1344+1571delinsAT
XM_006724101.4:c.1344+1570_1344+1571delinsAT	XP_006724164.1:n.1344+1570_1344+1571delinsAT
XM_006724102.2:c.888+1570_888+1571delinsAT	XP_006724165.1:n.888+1570_888+1571delinsAT
NM_001003681.3:c.1215+1570_1215+1571delinsAT MANE Select	NP_001003681.1:n.1215+1570_1215+1571delinsAT
NM_001362972.2:c.888+1570_888+1571delinsAT	NP_001349901.1:n.888+1570_888+1571delinsAT
NR_027780.2:n.1463+1570_1463+1571delinsAT