Canonical Allele Identifier: CA2403319415

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35266993_35266998delinsAAAAAG , CM000684.2:g.35266993_35266998delinsAAAAAG	GRCh38
NC_000022.10:g.35662986_35662991delinsAAAAAG , CM000684.1:g.35662986_35662991delinsAAAAAG	GRCh37
NC_000022.9:g.33992986_33992991delinsAAAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1390_1215+1395delinsAAAAAG MANE Select	ENSP00000216106.5:n.1215+1390_1215+1395delinsAAAAAG
ENST00000216106.5:c.1215+1390_1215+1395delinsAAAAAG	ENSP00000216106.5:n.1215+1390_1215+1395delinsAAAAAG
ENST00000418170.5:c.*1051+1390_*1051+1395delinsAAAAAG	ENSP00000395532.1:n.*1051+1390_*1051+1395delinsAAAAAG
NM_001003681.2:c.1215+1390_1215+1395delinsAAAAAG	NP_001003681.1:n.1215+1390_1215+1395delinsAAAAAG
NR_027780.1:n.1504+1390_1504+1395delinsAAAAAG
XM_006724100.2:c.1344+1390_1344+1395delinsAAAAAG	XP_006724163.1:n.1344+1390_1344+1395delinsAAAAAG
XM_006724101.2:c.1344+1390_1344+1395delinsAAAAAG	XP_006724164.1:n.1344+1390_1344+1395delinsAAAAAG
XM_006724102.1:c.888+1390_888+1395delinsAAAAAG	XP_006724165.1:n.888+1390_888+1395delinsAAAAAG
XM_011529817.1:c.1215+1390_1215+1395delinsAAAAAG	XP_011528119.1:n.1215+1390_1215+1395delinsAAAAAG
NM_001362972.1:c.888+1390_888+1395delinsAAAAAG	NP_001349901.1:n.888+1390_888+1395delinsAAAAAG
XM_006724100.4:c.1344+1390_1344+1395delinsAAAAAG	XP_006724163.1:n.1344+1390_1344+1395delinsAAAAAG
XM_006724101.4:c.1344+1390_1344+1395delinsAAAAAG	XP_006724164.1:n.1344+1390_1344+1395delinsAAAAAG
XM_006724102.2:c.888+1390_888+1395delinsAAAAAG	XP_006724165.1:n.888+1390_888+1395delinsAAAAAG
NM_001003681.3:c.1215+1390_1215+1395delinsAAAAAG MANE Select	NP_001003681.1:n.1215+1390_1215+1395delinsAAAAAG
NM_001362972.2:c.888+1390_888+1395delinsAAAAAG	NP_001349901.1:n.888+1390_888+1395delinsAAAAAG
NR_027780.2:n.1463+1390_1463+1395delinsAAAAAG