Canonical Allele Identifier: CA2818850920

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267212_35267216del , CM000684.2:g.35267212_35267216del	GRCh38
NC_000022.10:g.35663205_35663209del , CM000684.1:g.35663205_35663209del	GRCh37
NC_000022.9:g.33993205_33993209del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1609_1215+1613del MANE Select	ENSP00000216106.5:n.1215+1609_1215+1613del
ENST00000216106.5:c.1215+1609_1215+1613del	ENSP00000216106.5:n.1215+1609_1215+1613del
ENST00000418170.5:c.*1051+1609_*1051+1613del	ENSP00000395532.1:n.*1051+1609_*1051+1613del
NM_001003681.2:c.1215+1609_1215+1613del	NP_001003681.1:n.1215+1609_1215+1613del
NR_027780.1:n.1504+1609_1504+1613del
XM_006724100.2:c.1344+1609_1344+1613del	XP_006724163.1:n.1344+1609_1344+1613del
XM_006724101.2:c.1344+1609_1344+1613del	XP_006724164.1:n.1344+1609_1344+1613del
XM_006724102.1:c.888+1609_888+1613del	XP_006724165.1:n.888+1609_888+1613del
XM_011529817.1:c.1215+1609_1215+1613del	XP_011528119.1:n.1215+1609_1215+1613del
NM_001362972.1:c.888+1609_888+1613del	NP_001349901.1:n.888+1609_888+1613del
XM_006724100.4:c.1344+1609_1344+1613del	XP_006724163.1:n.1344+1609_1344+1613del
XM_006724101.4:c.1344+1609_1344+1613del	XP_006724164.1:n.1344+1609_1344+1613del
XM_006724102.2:c.888+1609_888+1613del	XP_006724165.1:n.888+1609_888+1613del
NM_001003681.3:c.1215+1609_1215+1613del MANE Select	NP_001003681.1:n.1215+1609_1215+1613del
NM_001362972.2:c.888+1609_888+1613del	NP_001349901.1:n.888+1609_888+1613del
NR_027780.2:n.1463+1609_1463+1613del