Canonical Allele Identifier: CA2738051543

Gene: HMGXB4

Linked Data

• dbSNP Id: rs2146408001

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267100_35267109del , CM000684.2:g.35267100_35267109del	GRCh38
NC_000022.10:g.35663093_35663102del , CM000684.1:g.35663093_35663102del	GRCh37
NC_000022.9:g.33993093_33993102del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1497_1215+1506del MANE Select	ENSP00000216106.5:n.1215+1497_1215+1506del
ENST00000216106.5:c.1215+1497_1215+1506del	ENSP00000216106.5:n.1215+1497_1215+1506del
ENST00000418170.5:c.*1051+1497_*1051+1506del	ENSP00000395532.1:n.*1051+1497_*1051+1506del
NM_001003681.2:c.1215+1497_1215+1506del	NP_001003681.1:n.1215+1497_1215+1506del
NR_027780.1:n.1504+1497_1504+1506del
XM_006724100.2:c.1344+1497_1344+1506del	XP_006724163.1:n.1344+1497_1344+1506del
XM_006724101.2:c.1344+1497_1344+1506del	XP_006724164.1:n.1344+1497_1344+1506del
XM_006724102.1:c.888+1497_888+1506del	XP_006724165.1:n.888+1497_888+1506del
XM_011529817.1:c.1215+1497_1215+1506del	XP_011528119.1:n.1215+1497_1215+1506del
NM_001362972.1:c.888+1497_888+1506del	NP_001349901.1:n.888+1497_888+1506del
XM_006724100.4:c.1344+1497_1344+1506del	XP_006724163.1:n.1344+1497_1344+1506del
XM_006724101.4:c.1344+1497_1344+1506del	XP_006724164.1:n.1344+1497_1344+1506del
XM_006724102.2:c.888+1497_888+1506del	XP_006724165.1:n.888+1497_888+1506del
NM_001003681.3:c.1215+1497_1215+1506del MANE Select	NP_001003681.1:n.1215+1497_1215+1506del
NM_001362972.2:c.888+1497_888+1506del	NP_001349901.1:n.888+1497_888+1506del
NR_027780.2:n.1463+1497_1463+1506del