Canonical Allele Identifier: CA402188637

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31323707T>C (hg19) ; chr18:g.33743743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743743T>C , CM000680.2:g.33743743T>C	GRCh38
NC_000018.9:g.31323707T>C , CM000680.1:g.31323707T>C	GRCh37
NC_000018.8:g.29577705T>C	NCBI36
NG_055244.1:g.170167T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3898T>C	ENSP00000513003.1:p.Cys1300Arg
ENST00000269197.12:c.3895T>C MANE Select	ENSP00000269197.4:p.Cys1299Arg
ENST00000681521.1:c.3775T>C	ENSP00000506037.1:p.Cys1259Arg
ENST00000269197.9:c.3895T>C	ENSP00000269197.4:p.Cys1299Arg
NM_030632.1:c.3895T>C	NP_085135.1:p.Cys1299Arg
XM_005258356.1:c.3898T>C	XP_005258413.1:p.Cys1300Arg
XM_011526205.1:c.3871T>C	XP_011524507.1:p.Cys1291Arg
XM_011526206.1:c.3817T>C	XP_011524508.1:p.Cys1273Arg
XM_011526207.1:c.3817T>C	XP_011524509.1:p.Cys1273Arg
XM_011526208.1:c.3778T>C	XP_011524510.1:p.Cys1260Arg
XM_011526209.1:c.3727T>C	XP_011524511.1:p.Cys1243Arg
XM_011526210.1:c.3727T>C	XP_011524512.1:p.Cys1243Arg
XM_011526211.1:c.3727T>C	XP_011524513.1:p.Cys1243Arg
XM_011526212.1:c.3727T>C	XP_011524514.1:p.Cys1243Arg
XM_011526213.1:c.3727T>C	XP_011524515.1:p.Cys1243Arg
XM_011526214.1:c.3727T>C	XP_011524516.1:p.Cys1243Arg
XM_011526215.1:c.859T>C	XP_011524517.1:p.Cys287Arg
NM_030632.2:c.3895T>C	NP_085135.1:p.Cys1299Arg
XM_011526205.2:c.3871T>C	XP_011524507.1:p.Cys1291Arg
XM_011526206.2:c.3817T>C	XP_011524508.1:p.Cys1273Arg
XM_011526213.2:c.3727T>C	XP_011524515.1:p.Cys1243Arg
XM_017026012.1:c.3817T>C	XP_016881501.1:p.Cys1273Arg
XM_017026013.1:c.3727T>C	XP_016881502.1:p.Cys1243Arg
XM_017026014.2:c.3727T>C	XP_016881503.1:p.Cys1243Arg
XM_024451269.1:c.3727T>C	XP_024307037.1:p.Cys1243Arg
NM_030632.3:c.3895T>C MANE Select	NP_085135.1:p.Cys1299Arg