Canonical Allele Identifier: CA2576484146

Gene: ASXL3

Linked Data

• gnomAD v4: 18-33744046-TCTGTAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744048_33744053del , CM000680.2:g.33744048_33744053del	GRCh38
NC_000018.9:g.31324012_31324017del , CM000680.1:g.31324012_31324017del	GRCh37
NC_000018.8:g.29578010_29578015del	NCBI36
NG_055244.1:g.170472_170477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4203_4208del	ENSP00000513003.1:p.Val1402_Ala1403del
ENST00000269197.12:c.4200_4205del MANE Select	ENSP00000269197.4:p.Val1401_Ala1402del
ENST00000681521.1:c.4080_4085del	ENSP00000506037.1:p.Val1361_Ala1362del
ENST00000269197.9:c.4200_4205del	ENSP00000269197.4:p.Val1401_Ala1402del
NM_030632.1:c.4200_4205del	NP_085135.1:p.Val1401_Ala1402del
XM_005258356.1:c.4203_4208del	XP_005258413.1:p.Val1402_Ala1403del
XM_011526205.1:c.4176_4181del	XP_011524507.1:p.Val1393_Ala1394del
XM_011526206.1:c.4122_4127del	XP_011524508.1:p.Val1375_Ala1376del
XM_011526207.1:c.4122_4127del	XP_011524509.1:p.Val1375_Ala1376del
XM_011526208.1:c.4083_4088del	XP_011524510.1:p.Val1362_Ala1363del
XM_011526209.1:c.4032_4037del	XP_011524511.1:p.Val1345_Ala1346del
XM_011526210.1:c.4032_4037del	XP_011524512.1:p.Val1345_Ala1346del
XM_011526211.1:c.4032_4037del	XP_011524513.1:p.Val1345_Ala1346del
XM_011526212.1:c.4032_4037del	XP_011524514.1:p.Val1345_Ala1346del
XM_011526213.1:c.4032_4037del	XP_011524515.1:p.Val1345_Ala1346del
XM_011526214.1:c.4032_4037del	XP_011524516.1:p.Val1345_Ala1346del
XM_011526215.1:c.1164_1169del	XP_011524517.1:p.Val389_Ala390del
NM_030632.2:c.4200_4205del	NP_085135.1:p.Val1401_Ala1402del
XM_011526205.2:c.4176_4181del	XP_011524507.1:p.Val1393_Ala1394del
XM_011526206.2:c.4122_4127del	XP_011524508.1:p.Val1375_Ala1376del
XM_011526213.2:c.4032_4037del	XP_011524515.1:p.Val1345_Ala1346del
XM_017026012.1:c.4122_4127del	XP_016881501.1:p.Val1375_Ala1376del
XM_017026013.1:c.4032_4037del	XP_016881502.1:p.Val1345_Ala1346del
XM_017026014.2:c.4032_4037del	XP_016881503.1:p.Val1345_Ala1346del
XM_024451269.1:c.4032_4037del	XP_024307037.1:p.Val1345_Ala1346del
NM_030632.3:c.4200_4205del MANE Select	NP_085135.1:p.Val1401_Ala1402del