Canonical Allele Identifier: CA323502763

Gene: HMGXB4

Linked Data

• dbSNP Id: rs759721920
• gnomAD v3: 22-35267026-TTGATCTC-T
• gnomAD v4: 22-35267026-TTGATCTC-T
• MyVariant Identifiers: chr22:g.35663020_35663026del (hg19) ; chr22:g.35267027_35267033del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267030_35267036del , CM000684.2:g.35267030_35267036del	GRCh38
NC_000022.10:g.35663023_35663029del , CM000684.1:g.35663023_35663029del	GRCh37
NC_000022.9:g.33993023_33993029del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1427_1215+1433del MANE Select	ENSP00000216106.5:n.1215+1427_1215+1433del
ENST00000216106.5:c.1215+1427_1215+1433del	ENSP00000216106.5:n.1215+1427_1215+1433del
ENST00000418170.5:c.*1051+1427_*1051+1433del	ENSP00000395532.1:n.*1051+1427_*1051+1433del
NM_001003681.2:c.1215+1427_1215+1433del	NP_001003681.1:n.1215+1427_1215+1433del
NR_027780.1:n.1504+1427_1504+1433del
XM_006724100.2:c.1344+1427_1344+1433del	XP_006724163.1:n.1344+1427_1344+1433del
XM_006724101.2:c.1344+1427_1344+1433del	XP_006724164.1:n.1344+1427_1344+1433del
XM_006724102.1:c.888+1427_888+1433del	XP_006724165.1:n.888+1427_888+1433del
XM_011529817.1:c.1215+1427_1215+1433del	XP_011528119.1:n.1215+1427_1215+1433del
NM_001362972.1:c.888+1427_888+1433del	NP_001349901.1:n.888+1427_888+1433del
XM_006724100.4:c.1344+1427_1344+1433del	XP_006724163.1:n.1344+1427_1344+1433del
XM_006724101.4:c.1344+1427_1344+1433del	XP_006724164.1:n.1344+1427_1344+1433del
XM_006724102.2:c.888+1427_888+1433del	XP_006724165.1:n.888+1427_888+1433del
NM_001003681.3:c.1215+1427_1215+1433del MANE Select	NP_001003681.1:n.1215+1427_1215+1433del
NM_001362972.2:c.888+1427_888+1433del	NP_001349901.1:n.888+1427_888+1433del
NR_027780.2:n.1463+1427_1463+1433del