Canonical Allele Identifier: CA402190700

Gene: ASXL3

Linked Data

• ClinVar Variation Id: 870739
• ClinVar RCV Id: RCV001090346
• dbSNP Id: rs1213246318
• MyVariant Identifiers: chr18:g.31324150G>T (hg19) ; chr18:g.33744186G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744186G>T , CM000680.2:g.33744186G>T	GRCh38
NC_000018.9:g.31324150G>T , CM000680.1:g.31324150G>T	GRCh37
NC_000018.8:g.29578148G>T	NCBI36
NG_055244.1:g.170610G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4341G>T	ENSP00000513003.1:p.Arg1447Ser
ENST00000269197.12:c.4338G>T MANE Select	ENSP00000269197.4:p.Arg1446Ser
ENST00000681521.1:c.4218G>T	ENSP00000506037.1:p.Arg1406Ser
ENST00000269197.9:c.4338G>T	ENSP00000269197.4:p.Arg1446Ser
NM_030632.1:c.4338G>T	NP_085135.1:p.Arg1446Ser
XM_005258356.1:c.4341G>T	XP_005258413.1:p.Arg1447Ser
XM_011526205.1:c.4314G>T	XP_011524507.1:p.Arg1438Ser
XM_011526206.1:c.4260G>T	XP_011524508.1:p.Arg1420Ser
XM_011526207.1:c.4260G>T	XP_011524509.1:p.Arg1420Ser
XM_011526208.1:c.4221G>T	XP_011524510.1:p.Arg1407Ser
XM_011526209.1:c.4170G>T	XP_011524511.1:p.Arg1390Ser
XM_011526210.1:c.4170G>T	XP_011524512.1:p.Arg1390Ser
XM_011526211.1:c.4170G>T	XP_011524513.1:p.Arg1390Ser
XM_011526212.1:c.4170G>T	XP_011524514.1:p.Arg1390Ser
XM_011526213.1:c.4170G>T	XP_011524515.1:p.Arg1390Ser
XM_011526214.1:c.4170G>T	XP_011524516.1:p.Arg1390Ser
XM_011526215.1:c.1302G>T	XP_011524517.1:p.Arg434Ser
NM_030632.2:c.4338G>T	NP_085135.1:p.Arg1446Ser
XM_011526205.2:c.4314G>T	XP_011524507.1:p.Arg1438Ser
XM_011526206.2:c.4260G>T	XP_011524508.1:p.Arg1420Ser
XM_011526213.2:c.4170G>T	XP_011524515.1:p.Arg1390Ser
XM_017026012.1:c.4260G>T	XP_016881501.1:p.Arg1420Ser
XM_017026013.1:c.4170G>T	XP_016881502.1:p.Arg1390Ser
XM_017026014.2:c.4170G>T	XP_016881503.1:p.Arg1390Ser
XM_024451269.1:c.4170G>T	XP_024307037.1:p.Arg1390Ser
NM_030632.3:c.4338G>T MANE Select	NP_085135.1:p.Arg1446Ser