Canonical Allele Identifier: CA402185192

Gene: ASXL3

Linked Data

• MyVariant Identifiers: chr18:g.31323179A>T (hg19) ; chr18:g.33743215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743215A>T , CM000680.2:g.33743215A>T	GRCh38
NC_000018.9:g.31323179A>T , CM000680.1:g.31323179A>T	GRCh37
NC_000018.8:g.29577177A>T	NCBI36
NG_055244.1:g.169639A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.3370A>T	ENSP00000513003.1:p.Thr1124Ser
ENST00000269197.12:c.3367A>T MANE Select	ENSP00000269197.4:p.Thr1123Ser
ENST00000592288.6:c.*2491A>T	ENSP00000465053.1:n.*2491A>T
ENST00000592541.6:c.*3026A>T	ENSP00000466655.2:n.*3026A>T
ENST00000593195.6:c.3579A>T	ENSP00000466073.1:n.3579A>T
ENST00000642541.1:c.3199A>T	ENSP00000493665.1:p.Thr1067Ser
ENST00000681521.1:c.3247A>T	ENSP00000506037.1:p.Thr1083Ser
ENST00000269197.9:c.3367A>T	ENSP00000269197.4:p.Thr1123Ser
ENST00000592288.5:c.*2491A>T	ENSP00000465053.1:n.*2491A>T
NM_030632.1:c.3367A>T	NP_085135.1:p.Thr1123Ser
XM_005258356.1:c.3370A>T	XP_005258413.1:p.Thr1124Ser
XM_011526205.1:c.3343A>T	XP_011524507.1:p.Thr1115Ser
XM_011526206.1:c.3289A>T	XP_011524508.1:p.Thr1097Ser
XM_011526207.1:c.3289A>T	XP_011524509.1:p.Thr1097Ser
XM_011526208.1:c.3250A>T	XP_011524510.1:p.Thr1084Ser
XM_011526209.1:c.3199A>T	XP_011524511.1:p.Thr1067Ser
XM_011526210.1:c.3199A>T	XP_011524512.1:p.Thr1067Ser
XM_011526211.1:c.3199A>T	XP_011524513.1:p.Thr1067Ser
XM_011526212.1:c.3199A>T	XP_011524514.1:p.Thr1067Ser
XM_011526213.1:c.3199A>T	XP_011524515.1:p.Thr1067Ser
XM_011526214.1:c.3199A>T	XP_011524516.1:p.Thr1067Ser
XM_011526215.1:c.331A>T	XP_011524517.1:p.Thr111Ser
NM_030632.2:c.3367A>T	NP_085135.1:p.Thr1123Ser
XM_011526205.2:c.3343A>T	XP_011524507.1:p.Thr1115Ser
XM_011526206.2:c.3289A>T	XP_011524508.1:p.Thr1097Ser
XM_011526213.2:c.3199A>T	XP_011524515.1:p.Thr1067Ser
XM_017026012.1:c.3289A>T	XP_016881501.1:p.Thr1097Ser
XM_017026013.1:c.3199A>T	XP_016881502.1:p.Thr1067Ser
XM_017026014.2:c.3199A>T	XP_016881503.1:p.Thr1067Ser
XM_024451269.1:c.3199A>T	XP_024307037.1:p.Thr1067Ser
NM_030632.3:c.3367A>T MANE Select	NP_085135.1:p.Thr1123Ser