Canonical Allele Identifier: CA2738051790

Gene: HMGXB4

Linked Data

• dbSNP Id: rs2146408623

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267339_35267340del , CM000684.2:g.35267339_35267340del	GRCh38
NC_000022.10:g.35663332_35663333del , CM000684.1:g.35663332_35663333del	GRCh37
NC_000022.9:g.33993332_33993333del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1736_1215+1737del MANE Select	ENSP00000216106.5:n.1215+1736_1215+1737del
ENST00000216106.5:c.1215+1736_1215+1737del	ENSP00000216106.5:n.1215+1736_1215+1737del
ENST00000418170.5:c.*1051+1736_*1051+1737del	ENSP00000395532.1:n.*1051+1736_*1051+1737del
NM_001003681.2:c.1215+1736_1215+1737del	NP_001003681.1:n.1215+1736_1215+1737del
NR_027780.1:n.1504+1736_1504+1737del
XM_006724100.2:c.1344+1736_1344+1737del	XP_006724163.1:n.1344+1736_1344+1737del
XM_006724101.2:c.1344+1736_1344+1737del	XP_006724164.1:n.1344+1736_1344+1737del
XM_006724102.1:c.888+1736_888+1737del	XP_006724165.1:n.888+1736_888+1737del
XM_011529817.1:c.1215+1736_1215+1737del	XP_011528119.1:n.1215+1736_1215+1737del
NM_001362972.1:c.888+1736_888+1737del	NP_001349901.1:n.888+1736_888+1737del
XM_006724100.4:c.1344+1736_1344+1737del	XP_006724163.1:n.1344+1736_1344+1737del
XM_006724101.4:c.1344+1736_1344+1737del	XP_006724164.1:n.1344+1736_1344+1737del
XM_006724102.2:c.888+1736_888+1737del	XP_006724165.1:n.888+1736_888+1737del
NM_001003681.3:c.1215+1736_1215+1737del MANE Select	NP_001003681.1:n.1215+1736_1215+1737del
NM_001362972.2:c.888+1736_888+1737del	NP_001349901.1:n.888+1736_888+1737del
NR_027780.2:n.1463+1736_1463+1737del