Canonical Allele Identifier: CA2294857526

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743025_33743040delinsCCGGGCCCAACAAGCT , CM000680.2:g.33743025_33743040delinsCCGGGCCCAACAAGCT	GRCh38
NC_000018.9:g.31322989_31323004delinsCCGGGCCCAACAAGCT , CM000680.1:g.31322989_31323004delinsCCGGGCCCAACAAGCT	GRCh37
NC_000018.8:g.29576987_29577002delinsCCGGGCCCAACAAGCT	NCBI36
NG_055244.1:g.169449_169464delinsCCGGGCCCAACAAGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.3180_3195delinsCCGGGCCCAACAAGCT	ENSP00000513003.1:p.Ala1060=
ENST00000269197.12:c.3177_3192delinsCCGGGCCCAACAAGCT MANE Select	ENSP00000269197.4:p.Ala1059=
ENST00000592288.6:c.*2301_*2316delinsCCGGGCCCAACAAGCT	ENSP00000465053.1:n.*2301_*2316delinsCCGGGCCCAACAAGCT
ENST00000592541.6:c.*2836_*2851delinsCCGGGCCCAACAAGCT	ENSP00000466655.2:n.*2836_*2851delinsCCGGGCCCAACAAGCT
ENST00000593195.6:c.3389_3404delinsCCGGGCCCAACAAGCT	ENSP00000466073.1:n.3389_3404delinsCCGGGCCCAACAAGCT
ENST00000642541.1:c.3009_3024delinsCCGGGCCCAACAAGCT	ENSP00000493665.1:p.Ala1003=
ENST00000681521.1:c.3057_3072delinsCCGGGCCCAACAAGCT	ENSP00000506037.1:p.Ala1019=
ENST00000269197.9:c.3177_3192delinsCCGGGCCCAACAAGCT	ENSP00000269197.4:p.Ala1059=
ENST00000592288.5:c.*2301_*2316delinsCCGGGCCCAACAAGCT	ENSP00000465053.1:n.*2301_*2316delinsCCGGGCCCAACAAGCT
NM_030632.1:c.3177_3192delinsCCGGGCCCAACAAGCT	NP_085135.1:p.Ala1059=
XM_005258356.1:c.3180_3195delinsCCGGGCCCAACAAGCT	XP_005258413.1:p.Ala1060=
XM_011526205.1:c.3153_3168delinsCCGGGCCCAACAAGCT	XP_011524507.1:p.Ala1051=
XM_011526206.1:c.3099_3114delinsCCGGGCCCAACAAGCT	XP_011524508.1:p.Ala1033=
XM_011526207.1:c.3099_3114delinsCCGGGCCCAACAAGCT	XP_011524509.1:p.Ala1033=
XM_011526208.1:c.3060_3075delinsCCGGGCCCAACAAGCT	XP_011524510.1:p.Ala1020=
XM_011526209.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524511.1:p.Ala1003=
XM_011526210.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524512.1:p.Ala1003=
XM_011526211.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524513.1:p.Ala1003=
XM_011526212.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524514.1:p.Ala1003=
XM_011526213.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524515.1:p.Ala1003=
XM_011526214.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524516.1:p.Ala1003=
XM_011526215.1:c.141_156delinsCCGGGCCCAACAAGCT	XP_011524517.1:p.Ala47=
NM_030632.2:c.3177_3192delinsCCGGGCCCAACAAGCT	NP_085135.1:p.Ala1059=
XM_011526205.2:c.3153_3168delinsCCGGGCCCAACAAGCT	XP_011524507.1:p.Ala1051=
XM_011526206.2:c.3099_3114delinsCCGGGCCCAACAAGCT	XP_011524508.1:p.Ala1033=
XM_011526213.2:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_011524515.1:p.Ala1003=
XM_017026012.1:c.3099_3114delinsCCGGGCCCAACAAGCT	XP_016881501.1:p.Ala1033=
XM_017026013.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_016881502.1:p.Ala1003=
XM_017026014.2:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_016881503.1:p.Ala1003=
XM_024451269.1:c.3009_3024delinsCCGGGCCCAACAAGCT	XP_024307037.1:p.Ala1003=
NM_030632.3:c.3177_3192delinsCCGGGCCCAACAAGCT MANE Select	NP_085135.1:p.Ala1059=