Canonical Allele Identifier: CA2403319700

Gene: HMGXB4

Linked Data

• dbSNP Id: rs1923338303

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267495_35267496del , CM000684.2:g.35267495_35267496del	GRCh38
NC_000022.10:g.35663488_35663489del , CM000684.1:g.35663488_35663489del	GRCh37
NC_000022.9:g.33993488_33993489del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1892_1215+1893del MANE Select	ENSP00000216106.5:n.1215+1892_1215+1893del
ENST00000216106.5:c.1215+1892_1215+1893del	ENSP00000216106.5:n.1215+1892_1215+1893del
ENST00000418170.5:c.*1051+1892_*1051+1893del	ENSP00000395532.1:n.*1051+1892_*1051+1893del
NM_001003681.2:c.1215+1892_1215+1893del	NP_001003681.1:n.1215+1892_1215+1893del
NR_027780.1:n.1504+1892_1504+1893del
XM_006724100.2:c.1344+1892_1344+1893del	XP_006724163.1:n.1344+1892_1344+1893del
XM_006724101.2:c.1344+1892_1344+1893del	XP_006724164.1:n.1344+1892_1344+1893del
XM_006724102.1:c.888+1892_888+1893del	XP_006724165.1:n.888+1892_888+1893del
XM_011529817.1:c.1215+1892_1215+1893del	XP_011528119.1:n.1215+1892_1215+1893del
NM_001362972.1:c.888+1892_888+1893del	NP_001349901.1:n.888+1892_888+1893del
XM_006724100.4:c.1344+1892_1344+1893del	XP_006724163.1:n.1344+1892_1344+1893del
XM_006724101.4:c.1344+1892_1344+1893del	XP_006724164.1:n.1344+1892_1344+1893del
XM_006724102.2:c.888+1892_888+1893del	XP_006724165.1:n.888+1892_888+1893del
NM_001003681.3:c.1215+1892_1215+1893del MANE Select	NP_001003681.1:n.1215+1892_1215+1893del
NM_001362972.2:c.888+1892_888+1893del	NP_001349901.1:n.888+1892_888+1893del
NR_027780.2:n.1463+1892_1463+1893del