Canonical Allele Identifier: CA915951347

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33736199_33741395del , CM000680.2:g.33736199_33741395del	GRCh38
NC_000018.9:g.31316163_31321359del , CM000680.1:g.31316163_31321359del	GRCh37
NC_000018.8:g.29570161_29575357del	NCBI36
NG_055244.1:g.162623_167819del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.1085+1784_3042+952del
ENST00000269197.12:c.1082+1784_3039+952del
ENST00000592288.6:c.*206+1784_*2163+952del
ENST00000592541.6:c.*741+1784_*2698+952del
ENST00000593195.6:c.1294+1784_3251+952del
ENST00000642541.1:c.914+1784_2871+952del
ENST00000681521.1:c.962+1784_2919+952del
ENST00000269197.9:c.1082+1784_3039+952del
ENST00000592288.5:c.*206+1784_*2163+952del
NM_030632.1:c.1082+1784_3039+952del
XM_005258356.1:c.1085+1784_3042+952del
XM_011526205.1:c.1058+1784_3015+952del
XM_011526206.1:c.1004+1784_2961+952del
XM_011526207.1:c.1004+1784_2961+952del
XM_011526208.1:c.965+1784_2922+952del
XM_011526209.1:c.914+1784_2871+952del
XM_011526210.1:c.914+1784_2871+952del
XM_011526211.1:c.914+1784_2871+952del
XM_011526212.1:c.914+1784_2871+952del
XM_011526213.1:c.914+1784_2871+952del
XM_011526214.1:c.914+1784_2871+952del
NM_030632.2:c.1082+1784_3039+952del
XM_011526205.2:c.1058+1784_3015+952del
XM_011526206.2:c.1004+1784_2961+952del
XM_011526213.2:c.914+1784_2871+952del
XM_017026012.1:c.1004+1784_2961+952del
XM_017026013.1:c.914+1784_2871+952del
XM_017026014.2:c.914+1784_2871+952del
XM_024451269.1:c.914+1784_2871+952del
NM_030632.3:c.1082+1784_3039+952del