Canonical Allele Identifier: CA402191123

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31324338C>T (hg19) ; chr18:g.33744374C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744374C>T , CM000680.2:g.33744374C>T	GRCh38
NC_000018.9:g.31324338C>T , CM000680.1:g.31324338C>T	GRCh37
NC_000018.8:g.29578336C>T	NCBI36
NG_055244.1:g.170798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4529C>T	ENSP00000513003.1:p.Ala1510Val
ENST00000269197.12:c.4526C>T MANE Select	ENSP00000269197.4:p.Ala1509Val
ENST00000681521.1:c.4406C>T	ENSP00000506037.1:p.Ala1469Val
ENST00000269197.9:c.4526C>T	ENSP00000269197.4:p.Ala1509Val
NM_030632.1:c.4526C>T	NP_085135.1:p.Ala1509Val
XM_005258356.1:c.4529C>T	XP_005258413.1:p.Ala1510Val
XM_011526205.1:c.4502C>T	XP_011524507.1:p.Ala1501Val
XM_011526206.1:c.4448C>T	XP_011524508.1:p.Ala1483Val
XM_011526207.1:c.4448C>T	XP_011524509.1:p.Ala1483Val
XM_011526208.1:c.4409C>T	XP_011524510.1:p.Ala1470Val
XM_011526209.1:c.4358C>T	XP_011524511.1:p.Ala1453Val
XM_011526210.1:c.4358C>T	XP_011524512.1:p.Ala1453Val
XM_011526211.1:c.4358C>T	XP_011524513.1:p.Ala1453Val
XM_011526212.1:c.4358C>T	XP_011524514.1:p.Ala1453Val
XM_011526213.1:c.4358C>T	XP_011524515.1:p.Ala1453Val
XM_011526214.1:c.4358C>T	XP_011524516.1:p.Ala1453Val
XM_011526215.1:c.1490C>T	XP_011524517.1:p.Ala497Val
NM_030632.2:c.4526C>T	NP_085135.1:p.Ala1509Val
XM_011526205.2:c.4502C>T	XP_011524507.1:p.Ala1501Val
XM_011526206.2:c.4448C>T	XP_011524508.1:p.Ala1483Val
XM_011526213.2:c.4358C>T	XP_011524515.1:p.Ala1453Val
XM_017026012.1:c.4448C>T	XP_016881501.1:p.Ala1483Val
XM_017026013.1:c.4358C>T	XP_016881502.1:p.Ala1453Val
XM_017026014.2:c.4358C>T	XP_016881503.1:p.Ala1453Val
XM_024451269.1:c.4358C>T	XP_024307037.1:p.Ala1453Val
NM_030632.3:c.4526C>T MANE Select	NP_085135.1:p.Ala1509Val