Canonical Allele Identifier: CA323502965

Gene: HMGXB4

Linked Data

• dbSNP Id: rs1555887418
• MyVariant Identifiers: chr22:g.35663147_35663148insTATTATATG (hg19) ; chr22:g.35267154_35267155insTATTATATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.35267154_35267155insTATTATATG , CM000684.2:g.35267154_35267155insTATTATATG	GRCh38
NC_000022.10:g.35663147_35663148insTATTATATG , CM000684.1:g.35663147_35663148insTATTATATG	GRCh37
NC_000022.9:g.33993147_33993148insTATTATATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216106.6:c.1215+1551_1215+1552insTATTATATG MANE Select	ENSP00000216106.5:n.1215+1551_1215+1552insTATTATATG
ENST00000216106.5:c.1215+1551_1215+1552insTATTATATG	ENSP00000216106.5:n.1215+1551_1215+1552insTATTATATG
ENST00000418170.5:c.*1051+1551_*1051+1552insTATTATATG	ENSP00000395532.1:n.*1051+1551_*1051+1552insTATTATATG
NM_001003681.2:c.1215+1551_1215+1552insTATTATATG	NP_001003681.1:n.1215+1551_1215+1552insTATTATATG
NR_027780.1:n.1504+1551_1504+1552insTATTATATG
XM_006724100.2:c.1344+1551_1344+1552insTATTATATG	XP_006724163.1:n.1344+1551_1344+1552insTATTATATG
XM_006724101.2:c.1344+1551_1344+1552insTATTATATG	XP_006724164.1:n.1344+1551_1344+1552insTATTATATG
XM_006724102.1:c.888+1551_888+1552insTATTATATG	XP_006724165.1:n.888+1551_888+1552insTATTATATG
XM_011529817.1:c.1215+1551_1215+1552insTATTATATG	XP_011528119.1:n.1215+1551_1215+1552insTATTATATG
NM_001362972.1:c.888+1551_888+1552insTATTATATG	NP_001349901.1:n.888+1551_888+1552insTATTATATG
XM_006724100.4:c.1344+1551_1344+1552insTATTATATG	XP_006724163.1:n.1344+1551_1344+1552insTATTATATG
XM_006724101.4:c.1344+1551_1344+1552insTATTATATG	XP_006724164.1:n.1344+1551_1344+1552insTATTATATG
XM_006724102.2:c.888+1551_888+1552insTATTATATG	XP_006724165.1:n.888+1551_888+1552insTATTATATG
NM_001003681.3:c.1215+1551_1215+1552insTATTATATG MANE Select	NP_001003681.1:n.1215+1551_1215+1552insTATTATATG
NM_001362972.2:c.888+1551_888+1552insTATTATATG	NP_001349901.1:n.888+1551_888+1552insTATTATATG
NR_027780.2:n.1463+1551_1463+1552insTATTATATG