Canonical Allele Identifier: CA2641457611

Gene: ASXL3

Linked Data

• gnomAD v4: 18-33742748-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33742749_33742750dup , CM000680.2:g.33742749_33742750dup	GRCh38
NC_000018.9:g.31322713_31322714dup , CM000680.1:g.31322713_31322714dup	GRCh37
NC_000018.8:g.29576711_29576712dup	NCBI36
NG_055244.1:g.169173_169174dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3043-139_3043-138dup	ENSP00000513003.1:n.3043-139_3043-138dup
ENST00000269197.12:c.3040-139_3040-138dup MANE Select	ENSP00000269197.4:n.3040-139_3040-138dup
ENST00000592288.6:c.*2164-139_*2164-138dup	ENSP00000465053.1:n.*2164-139_*2164-138dup
ENST00000592541.6:c.*2699-139_*2699-138dup	ENSP00000466655.2:n.*2699-139_*2699-138dup
ENST00000593195.6:c.3252-139_3252-138dup	ENSP00000466073.1:n.3252-139_3252-138dup
ENST00000642541.1:c.2872-139_2872-138dup	ENSP00000493665.1:n.2872-139_2872-138dup
ENST00000681521.1:c.2920-139_2920-138dup	ENSP00000506037.1:n.2920-139_2920-138dup
ENST00000269197.9:c.3040-139_3040-138dup	ENSP00000269197.4:n.3040-139_3040-138dup
ENST00000592288.5:c.*2164-139_*2164-138dup	ENSP00000465053.1:n.*2164-139_*2164-138dup
NM_030632.1:c.3040-139_3040-138dup	NP_085135.1:n.3040-139_3040-138dup
XM_005258356.1:c.3043-139_3043-138dup	XP_005258413.1:n.3043-139_3043-138dup
XM_011526205.1:c.3016-139_3016-138dup	XP_011524507.1:n.3016-139_3016-138dup
XM_011526206.1:c.2962-139_2962-138dup	XP_011524508.1:n.2962-139_2962-138dup
XM_011526207.1:c.2962-139_2962-138dup	XP_011524509.1:n.2962-139_2962-138dup
XM_011526208.1:c.2923-139_2923-138dup	XP_011524510.1:n.2923-139_2923-138dup
XM_011526209.1:c.2872-139_2872-138dup	XP_011524511.1:n.2872-139_2872-138dup
XM_011526210.1:c.2872-139_2872-138dup	XP_011524512.1:n.2872-139_2872-138dup
XM_011526211.1:c.2872-139_2872-138dup	XP_011524513.1:n.2872-139_2872-138dup
XM_011526212.1:c.2872-139_2872-138dup	XP_011524514.1:n.2872-139_2872-138dup
XM_011526213.1:c.2872-139_2872-138dup	XP_011524515.1:n.2872-139_2872-138dup
XM_011526214.1:c.2872-139_2872-138dup	XP_011524516.1:n.2872-139_2872-138dup
XM_011526215.1:c.4-139_4-138dup	XP_011524517.1:n.4-139_4-138dup
NM_030632.2:c.3040-139_3040-138dup	NP_085135.1:n.3040-139_3040-138dup
XM_011526205.2:c.3016-139_3016-138dup	XP_011524507.1:n.3016-139_3016-138dup
XM_011526206.2:c.2962-139_2962-138dup	XP_011524508.1:n.2962-139_2962-138dup
XM_011526213.2:c.2872-139_2872-138dup	XP_011524515.1:n.2872-139_2872-138dup
XM_017026012.1:c.2962-139_2962-138dup	XP_016881501.1:n.2962-139_2962-138dup
XM_017026013.1:c.2872-139_2872-138dup	XP_016881502.1:n.2872-139_2872-138dup
XM_017026014.2:c.2872-139_2872-138dup	XP_016881503.1:n.2872-139_2872-138dup
XM_024451269.1:c.2872-139_2872-138dup	XP_024307037.1:n.2872-139_2872-138dup
NM_030632.3:c.3040-139_3040-138dup MANE Select	NP_085135.1:n.3040-139_3040-138dup