Canonical Allele Identifier: CA752715602

Gene: HMGXB4

Linked Data

• dbSNP Id: rs1400006547
• MyVariant Identifiers: chr22:g.35663159_35663163del (hg19) ; chr22:g.35267166_35267170del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267169_35267173del , CM000684.2:g.35267169_35267173del	GRCh38
NC_000022.10:g.35663162_35663166del , CM000684.1:g.35663162_35663166del	GRCh37
NC_000022.9:g.33993162_33993166del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1566_1215+1570del MANE Select	ENSP00000216106.5:n.1215+1566_1215+1570del
ENST00000216106.5:c.1215+1566_1215+1570del	ENSP00000216106.5:n.1215+1566_1215+1570del
ENST00000418170.5:c.*1051+1566_*1051+1570del	ENSP00000395532.1:n.*1051+1566_*1051+1570del
NM_001003681.2:c.1215+1566_1215+1570del	NP_001003681.1:n.1215+1566_1215+1570del
NR_027780.1:n.1504+1566_1504+1570del
XM_006724100.2:c.1344+1566_1344+1570del	XP_006724163.1:n.1344+1566_1344+1570del
XM_006724101.2:c.1344+1566_1344+1570del	XP_006724164.1:n.1344+1566_1344+1570del
XM_006724102.1:c.888+1566_888+1570del	XP_006724165.1:n.888+1566_888+1570del
XM_011529817.1:c.1215+1566_1215+1570del	XP_011528119.1:n.1215+1566_1215+1570del
NM_001362972.1:c.888+1566_888+1570del	NP_001349901.1:n.888+1566_888+1570del
XM_006724100.4:c.1344+1566_1344+1570del	XP_006724163.1:n.1344+1566_1344+1570del
XM_006724101.4:c.1344+1566_1344+1570del	XP_006724164.1:n.1344+1566_1344+1570del
XM_006724102.2:c.888+1566_888+1570del	XP_006724165.1:n.888+1566_888+1570del
NM_001003681.3:c.1215+1566_1215+1570del MANE Select	NP_001003681.1:n.1215+1566_1215+1570del
NM_001362972.2:c.888+1566_888+1570del	NP_001349901.1:n.888+1566_888+1570del
NR_027780.2:n.1463+1566_1463+1570del