Canonical Allele Identifier: CA402184681

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31322978G>T (hg19) ; chr18:g.33743014G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743014G>T , CM000680.2:g.33743014G>T	GRCh38
NC_000018.9:g.31322978G>T , CM000680.1:g.31322978G>T	GRCh37
NC_000018.8:g.29576976G>T	NCBI36
NG_055244.1:g.169438G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3169G>T	ENSP00000513003.1:p.Asp1057Tyr
ENST00000269197.12:c.3166G>T MANE Select	ENSP00000269197.4:p.Asp1056Tyr
ENST00000592288.6:c.*2290G>T	ENSP00000465053.1:n.*2290G>T
ENST00000592541.6:c.*2825G>T	ENSP00000466655.2:n.*2825G>T
ENST00000593195.6:c.3378G>T	ENSP00000466073.1:n.3378G>T
ENST00000642541.1:c.2998G>T	ENSP00000493665.1:p.Asp1000Tyr
ENST00000681521.1:c.3046G>T	ENSP00000506037.1:p.Asp1016Tyr
ENST00000269197.9:c.3166G>T	ENSP00000269197.4:p.Asp1056Tyr
ENST00000592288.5:c.*2290G>T	ENSP00000465053.1:n.*2290G>T
NM_030632.1:c.3166G>T	NP_085135.1:p.Asp1056Tyr
XM_005258356.1:c.3169G>T	XP_005258413.1:p.Asp1057Tyr
XM_011526205.1:c.3142G>T	XP_011524507.1:p.Asp1048Tyr
XM_011526206.1:c.3088G>T	XP_011524508.1:p.Asp1030Tyr
XM_011526207.1:c.3088G>T	XP_011524509.1:p.Asp1030Tyr
XM_011526208.1:c.3049G>T	XP_011524510.1:p.Asp1017Tyr
XM_011526209.1:c.2998G>T	XP_011524511.1:p.Asp1000Tyr
XM_011526210.1:c.2998G>T	XP_011524512.1:p.Asp1000Tyr
XM_011526211.1:c.2998G>T	XP_011524513.1:p.Asp1000Tyr
XM_011526212.1:c.2998G>T	XP_011524514.1:p.Asp1000Tyr
XM_011526213.1:c.2998G>T	XP_011524515.1:p.Asp1000Tyr
XM_011526214.1:c.2998G>T	XP_011524516.1:p.Asp1000Tyr
XM_011526215.1:c.130G>T	XP_011524517.1:p.Asp44Tyr
NM_030632.2:c.3166G>T	NP_085135.1:p.Asp1056Tyr
XM_011526205.2:c.3142G>T	XP_011524507.1:p.Asp1048Tyr
XM_011526206.2:c.3088G>T	XP_011524508.1:p.Asp1030Tyr
XM_011526213.2:c.2998G>T	XP_011524515.1:p.Asp1000Tyr
XM_017026012.1:c.3088G>T	XP_016881501.1:p.Asp1030Tyr
XM_017026013.1:c.2998G>T	XP_016881502.1:p.Asp1000Tyr
XM_017026014.2:c.2998G>T	XP_016881503.1:p.Asp1000Tyr
XM_024451269.1:c.2998G>T	XP_024307037.1:p.Asp1000Tyr
NM_030632.3:c.3166G>T MANE Select	NP_085135.1:p.Asp1056Tyr