Canonical Allele Identifier: CA297793209

Gene: ASXL3

Linked Data

• dbSNP Id: rs370500804
• MyVariant Identifiers: chr18:g.31323674_31323675insC (hg19) ; chr18:g.33743710_33743711insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743711dup , CM000680.2:g.33743711dup	GRCh38
NC_000018.9:g.31323675dup , CM000680.1:g.31323675dup	GRCh37
NC_000018.8:g.29577673dup	NCBI36
NG_055244.1:g.170135dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3866dup	ENSP00000513003.1:p.Asp1290Ter
ENST00000269197.12:c.3863dup MANE Select	ENSP00000269197.4:p.Asp1289Ter
ENST00000681521.1:c.3743dup	ENSP00000506037.1:p.Asp1249Ter
ENST00000269197.9:c.3863dup	ENSP00000269197.4:p.Asp1289Ter
NM_030632.1:c.3863dup	NP_085135.1:p.Asp1289Ter
XM_005258356.1:c.3866dup	XP_005258413.1:p.Asp1290Ter
XM_011526205.1:c.3839dup	XP_011524507.1:p.Asp1281Ter
XM_011526206.1:c.3785dup	XP_011524508.1:p.Asp1263Ter
XM_011526207.1:c.3785dup	XP_011524509.1:p.Asp1263Ter
XM_011526208.1:c.3746dup	XP_011524510.1:p.Asp1250Ter
XM_011526209.1:c.3695dup	XP_011524511.1:p.Asp1233Ter
XM_011526210.1:c.3695dup	XP_011524512.1:p.Asp1233Ter
XM_011526211.1:c.3695dup	XP_011524513.1:p.Asp1233Ter
XM_011526212.1:c.3695dup	XP_011524514.1:p.Asp1233Ter
XM_011526213.1:c.3695dup	XP_011524515.1:p.Asp1233Ter
XM_011526214.1:c.3695dup	XP_011524516.1:p.Asp1233Ter
XM_011526215.1:c.827dup	XP_011524517.1:p.Asp277Ter
NM_030632.2:c.3863dup	NP_085135.1:p.Asp1289Ter
XM_011526205.2:c.3839dup	XP_011524507.1:p.Asp1281Ter
XM_011526206.2:c.3785dup	XP_011524508.1:p.Asp1263Ter
XM_011526213.2:c.3695dup	XP_011524515.1:p.Asp1233Ter
XM_017026012.1:c.3785dup	XP_016881501.1:p.Asp1263Ter
XM_017026013.1:c.3695dup	XP_016881502.1:p.Asp1233Ter
XM_017026014.2:c.3695dup	XP_016881503.1:p.Asp1233Ter
XM_024451269.1:c.3695dup	XP_024307037.1:p.Asp1233Ter
NM_030632.3:c.3863dup MANE Select	NP_085135.1:p.Asp1289Ter