Canonical Allele Identifier: CA2294857515

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33742992C= , CM000680.2:g.33742992C=	GRCh38
NC_000018.9:g.31322956C= , CM000680.1:g.31322956C=	GRCh37
NC_000018.8:g.29576954C=	NCBI36
NG_055244.1:g.169416C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.3147C=	ENSP00000513003.1:p.Asn1049=
ENST00000269197.12:c.3144C= MANE Select	ENSP00000269197.4:p.Asn1048=
ENST00000592288.6:c.*2268C=	ENSP00000465053.1:n.*2268C=
ENST00000592541.6:c.*2803C=	ENSP00000466655.2:n.*2803C=
ENST00000593195.6:c.3356C=	ENSP00000466073.1:n.3356C=
ENST00000642541.1:c.2976C=	ENSP00000493665.1:p.Asn992=
ENST00000681521.1:c.3024C=	ENSP00000506037.1:p.Asn1008=
ENST00000269197.9:c.3144C=	ENSP00000269197.4:p.Asn1048=
ENST00000592288.5:c.*2268C=	ENSP00000465053.1:n.*2268C=
NM_030632.1:c.3144C=	NP_085135.1:p.Asn1048=
XM_005258356.1:c.3147C=	XP_005258413.1:p.Asn1049=
XM_011526205.1:c.3120C=	XP_011524507.1:p.Asn1040=
XM_011526206.1:c.3066C=	XP_011524508.1:p.Asn1022=
XM_011526207.1:c.3066C=	XP_011524509.1:p.Asn1022=
XM_011526208.1:c.3027C=	XP_011524510.1:p.Asn1009=
XM_011526209.1:c.2976C=	XP_011524511.1:p.Asn992=
XM_011526210.1:c.2976C=	XP_011524512.1:p.Asn992=
XM_011526211.1:c.2976C=	XP_011524513.1:p.Asn992=
XM_011526212.1:c.2976C=	XP_011524514.1:p.Asn992=
XM_011526213.1:c.2976C=	XP_011524515.1:p.Asn992=
XM_011526214.1:c.2976C=	XP_011524516.1:p.Asn992=
XM_011526215.1:c.108C=	XP_011524517.1:p.Asn36=
NM_030632.2:c.3144C=	NP_085135.1:p.Asn1048=
XM_011526205.2:c.3120C=	XP_011524507.1:p.Asn1040=
XM_011526206.2:c.3066C=	XP_011524508.1:p.Asn1022=
XM_011526213.2:c.2976C=	XP_011524515.1:p.Asn992=
XM_017026012.1:c.3066C=	XP_016881501.1:p.Asn1022=
XM_017026013.1:c.2976C=	XP_016881502.1:p.Asn992=
XM_017026014.2:c.2976C=	XP_016881503.1:p.Asn992=
XM_024451269.1:c.2976C=	XP_024307037.1:p.Asn992=
NM_030632.3:c.3144C= MANE Select	NP_085135.1:p.Asn1048=