Canonical Allele Identifier: CA2403319488

Gene: HMGXB4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267130_35267132delinsATC , CM000684.2:g.35267130_35267132delinsATC	GRCh38
NC_000022.10:g.35663123_35663125delinsATC , CM000684.1:g.35663123_35663125delinsATC	GRCh37
NC_000022.9:g.33993123_33993125delinsATC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1527_1215+1529delinsATC MANE Select	ENSP00000216106.5:n.1215+1527_1215+1529delinsATC
ENST00000216106.5:c.1215+1527_1215+1529delinsATC	ENSP00000216106.5:n.1215+1527_1215+1529delinsATC
ENST00000418170.5:c.*1051+1527_*1051+1529delinsATC	ENSP00000395532.1:n.*1051+1527_*1051+1529delinsATC
NM_001003681.2:c.1215+1527_1215+1529delinsATC	NP_001003681.1:n.1215+1527_1215+1529delinsATC
NR_027780.1:n.1504+1527_1504+1529delinsATC
XM_006724100.2:c.1344+1527_1344+1529delinsATC	XP_006724163.1:n.1344+1527_1344+1529delinsATC
XM_006724101.2:c.1344+1527_1344+1529delinsATC	XP_006724164.1:n.1344+1527_1344+1529delinsATC
XM_006724102.1:c.888+1527_888+1529delinsATC	XP_006724165.1:n.888+1527_888+1529delinsATC
XM_011529817.1:c.1215+1527_1215+1529delinsATC	XP_011528119.1:n.1215+1527_1215+1529delinsATC
NM_001362972.1:c.888+1527_888+1529delinsATC	NP_001349901.1:n.888+1527_888+1529delinsATC
XM_006724100.4:c.1344+1527_1344+1529delinsATC	XP_006724163.1:n.1344+1527_1344+1529delinsATC
XM_006724101.4:c.1344+1527_1344+1529delinsATC	XP_006724164.1:n.1344+1527_1344+1529delinsATC
XM_006724102.2:c.888+1527_888+1529delinsATC	XP_006724165.1:n.888+1527_888+1529delinsATC
NM_001003681.3:c.1215+1527_1215+1529delinsATC MANE Select	NP_001003681.1:n.1215+1527_1215+1529delinsATC
NM_001362972.2:c.888+1527_888+1529delinsATC	NP_001349901.1:n.888+1527_888+1529delinsATC
NR_027780.2:n.1463+1527_1463+1529delinsATC