Canonical Allele Identifier: CA1139666016

Gene: ASXL3

Linked Data

• ClinVar Variation Id: 638608
• ClinVar RCV Id: RCV000791293

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33736196_33741393del , CM000680.2:g.33736196_33741393del	GRCh38
NC_000018.9:g.31316160_31321357del , CM000680.1:g.31316160_31321357del	GRCh37
NC_000018.8:g.29570158_29575355del	NCBI36
NG_055244.1:g.162620_167817del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.1085+1781_3042+950del
ENST00000269197.12:c.1082+1781_3039+950del
ENST00000592288.6:c.*206+1781_*2163+950del
ENST00000592541.6:c.*741+1781_*2698+950del
ENST00000593195.6:c.1294+1781_3251+950del
ENST00000642541.1:c.914+1781_2871+950del
ENST00000681521.1:c.962+1781_2919+950del
ENST00000269197.9:c.1082+1781_3039+950del
ENST00000592288.5:c.*206+1781_*2163+950del
NM_030632.1:c.1082+1781_3039+950del
XM_005258356.1:c.1085+1781_3042+950del
XM_011526205.1:c.1058+1781_3015+950del
XM_011526206.1:c.1004+1781_2961+950del
XM_011526207.1:c.1004+1781_2961+950del
XM_011526208.1:c.965+1781_2922+950del
XM_011526209.1:c.914+1781_2871+950del
XM_011526210.1:c.914+1781_2871+950del
XM_011526211.1:c.914+1781_2871+950del
XM_011526212.1:c.914+1781_2871+950del
XM_011526213.1:c.914+1781_2871+950del
XM_011526214.1:c.914+1781_2871+950del
NM_030632.2:c.1082+1781_3039+950del
XM_011526205.2:c.1058+1781_3015+950del
XM_011526206.2:c.1004+1781_2961+950del
XM_011526213.2:c.914+1781_2871+950del
XM_017026012.1:c.1004+1781_2961+950del
XM_017026013.1:c.914+1781_2871+950del
XM_017026014.2:c.914+1781_2871+950del
XM_024451269.1:c.914+1781_2871+950del
NM_030632.3:c.1082+1781_3039+950del