Canonical Allele Identifier: CA402175930

Gene: ASXL3

Linked Data

• ClinVar Variation Id: 1321784
• ClinVar RCV Id: RCV001779876
• dbSNP Id: rs2145412985
• MyVariant Identifiers: chr18:g.31318965G>T (hg19) ; chr18:g.33739001G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33739001G>T , CM000680.2:g.33739001G>T	GRCh38
NC_000018.9:g.31318965G>T , CM000680.1:g.31318965G>T	GRCh37
NC_000018.8:g.29572963G>T	NCBI36
NG_055244.1:g.165425G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.1600G>T	ENSP00000513003.1:p.Val534Phe
ENST00000269197.12:c.1597G>T MANE Select	ENSP00000269197.4:p.Val533Phe
ENST00000592288.6:c.*721G>T	ENSP00000465053.1:n.*721G>T
ENST00000592541.6:c.*1256G>T	ENSP00000466655.2:n.*1256G>T
ENST00000593195.6:c.1809G>T	ENSP00000466073.1:n.1809G>T
ENST00000642541.1:c.1429G>T	ENSP00000493665.1:p.Val477Phe
ENST00000681521.1:c.1477G>T	ENSP00000506037.1:p.Val493Phe
ENST00000269197.9:c.1597G>T	ENSP00000269197.4:p.Val533Phe
ENST00000592288.5:c.*721G>T	ENSP00000465053.1:n.*721G>T
NM_030632.1:c.1597G>T	NP_085135.1:p.Val533Phe
XM_005258356.1:c.1600G>T	XP_005258413.1:p.Val534Phe
XM_011526205.1:c.1573G>T	XP_011524507.1:p.Val525Phe
XM_011526206.1:c.1519G>T	XP_011524508.1:p.Val507Phe
XM_011526207.1:c.1519G>T	XP_011524509.1:p.Val507Phe
XM_011526208.1:c.1480G>T	XP_011524510.1:p.Val494Phe
XM_011526209.1:c.1429G>T	XP_011524511.1:p.Val477Phe
XM_011526210.1:c.1429G>T	XP_011524512.1:p.Val477Phe
XM_011526211.1:c.1429G>T	XP_011524513.1:p.Val477Phe
XM_011526212.1:c.1429G>T	XP_011524514.1:p.Val477Phe
XM_011526213.1:c.1429G>T	XP_011524515.1:p.Val477Phe
XM_011526214.1:c.1429G>T	XP_011524516.1:p.Val477Phe
NM_030632.2:c.1597G>T	NP_085135.1:p.Val533Phe
XM_011526205.2:c.1573G>T	XP_011524507.1:p.Val525Phe
XM_011526206.2:c.1519G>T	XP_011524508.1:p.Val507Phe
XM_011526213.2:c.1429G>T	XP_011524515.1:p.Val477Phe
XM_017026012.1:c.1519G>T	XP_016881501.1:p.Val507Phe
XM_017026013.1:c.1429G>T	XP_016881502.1:p.Val477Phe
XM_017026014.2:c.1429G>T	XP_016881503.1:p.Val477Phe
XM_024451269.1:c.1429G>T	XP_024307037.1:p.Val477Phe
NM_030632.3:c.1597G>T MANE Select	NP_085135.1:p.Val533Phe