Canonical Allele Identifier: CA2294858029

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744183C= , CM000680.2:g.33744183C=	GRCh38
NC_000018.9:g.31324147C= , CM000680.1:g.31324147C=	GRCh37
NC_000018.8:g.29578145C=	NCBI36
NG_055244.1:g.170607C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4338C=	ENSP00000513003.1:p.Asn1446=
ENST00000269197.12:c.4335C= MANE Select	ENSP00000269197.4:p.Asn1445=
ENST00000681521.1:c.4215C=	ENSP00000506037.1:p.Asn1405=
ENST00000269197.9:c.4335C=	ENSP00000269197.4:p.Asn1445=
NM_030632.1:c.4335C=	NP_085135.1:p.Asn1445=
XM_005258356.1:c.4338C=	XP_005258413.1:p.Asn1446=
XM_011526205.1:c.4311C=	XP_011524507.1:p.Asn1437=
XM_011526206.1:c.4257C=	XP_011524508.1:p.Asn1419=
XM_011526207.1:c.4257C=	XP_011524509.1:p.Asn1419=
XM_011526208.1:c.4218C=	XP_011524510.1:p.Asn1406=
XM_011526209.1:c.4167C=	XP_011524511.1:p.Asn1389=
XM_011526210.1:c.4167C=	XP_011524512.1:p.Asn1389=
XM_011526211.1:c.4167C=	XP_011524513.1:p.Asn1389=
XM_011526212.1:c.4167C=	XP_011524514.1:p.Asn1389=
XM_011526213.1:c.4167C=	XP_011524515.1:p.Asn1389=
XM_011526214.1:c.4167C=	XP_011524516.1:p.Asn1389=
XM_011526215.1:c.1299C=	XP_011524517.1:p.Asn433=
NM_030632.2:c.4335C=	NP_085135.1:p.Asn1445=
XM_011526205.2:c.4311C=	XP_011524507.1:p.Asn1437=
XM_011526206.2:c.4257C=	XP_011524508.1:p.Asn1419=
XM_011526213.2:c.4167C=	XP_011524515.1:p.Asn1389=
XM_017026012.1:c.4257C=	XP_016881501.1:p.Asn1419=
XM_017026013.1:c.4167C=	XP_016881502.1:p.Asn1389=
XM_017026014.2:c.4167C=	XP_016881503.1:p.Asn1389=
XM_024451269.1:c.4167C=	XP_024307037.1:p.Asn1389=
NM_030632.3:c.4335C= MANE Select	NP_085135.1:p.Asn1445=