Canonical Allele Identifier: CA2294858079

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744301_33744307delinsTTGTCTC , CM000680.2:g.33744301_33744307delinsTTGTCTC	GRCh38
NC_000018.9:g.31324265_31324271delinsTTGTCTC , CM000680.1:g.31324265_31324271delinsTTGTCTC	GRCh37
NC_000018.8:g.29578263_29578269delinsTTGTCTC	NCBI36
NG_055244.1:g.170725_170731delinsTTGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4456_4462delinsTTGTCTC	ENSP00000513003.1:p.Leu1486=
ENST00000269197.12:c.4453_4459delinsTTGTCTC MANE Select	ENSP00000269197.4:p.Leu1485=
ENST00000681521.1:c.4333_4339delinsTTGTCTC	ENSP00000506037.1:p.Leu1445=
ENST00000269197.9:c.4453_4459delinsTTGTCTC	ENSP00000269197.4:p.Leu1485=
NM_030632.1:c.4453_4459delinsTTGTCTC	NP_085135.1:p.Leu1485=
XM_005258356.1:c.4456_4462delinsTTGTCTC	XP_005258413.1:p.Leu1486=
XM_011526205.1:c.4429_4435delinsTTGTCTC	XP_011524507.1:p.Leu1477=
XM_011526206.1:c.4375_4381delinsTTGTCTC	XP_011524508.1:p.Leu1459=
XM_011526207.1:c.4375_4381delinsTTGTCTC	XP_011524509.1:p.Leu1459=
XM_011526208.1:c.4336_4342delinsTTGTCTC	XP_011524510.1:p.Leu1446=
XM_011526209.1:c.4285_4291delinsTTGTCTC	XP_011524511.1:p.Leu1429=
XM_011526210.1:c.4285_4291delinsTTGTCTC	XP_011524512.1:p.Leu1429=
XM_011526211.1:c.4285_4291delinsTTGTCTC	XP_011524513.1:p.Leu1429=
XM_011526212.1:c.4285_4291delinsTTGTCTC	XP_011524514.1:p.Leu1429=
XM_011526213.1:c.4285_4291delinsTTGTCTC	XP_011524515.1:p.Leu1429=
XM_011526214.1:c.4285_4291delinsTTGTCTC	XP_011524516.1:p.Leu1429=
XM_011526215.1:c.1417_1423delinsTTGTCTC	XP_011524517.1:p.Leu473=
NM_030632.2:c.4453_4459delinsTTGTCTC	NP_085135.1:p.Leu1485=
XM_011526205.2:c.4429_4435delinsTTGTCTC	XP_011524507.1:p.Leu1477=
XM_011526206.2:c.4375_4381delinsTTGTCTC	XP_011524508.1:p.Leu1459=
XM_011526213.2:c.4285_4291delinsTTGTCTC	XP_011524515.1:p.Leu1429=
XM_017026012.1:c.4375_4381delinsTTGTCTC	XP_016881501.1:p.Leu1459=
XM_017026013.1:c.4285_4291delinsTTGTCTC	XP_016881502.1:p.Leu1429=
XM_017026014.2:c.4285_4291delinsTTGTCTC	XP_016881503.1:p.Leu1429=
XM_024451269.1:c.4285_4291delinsTTGTCTC	XP_024307037.1:p.Leu1429=
NM_030632.3:c.4453_4459delinsTTGTCTC MANE Select	NP_085135.1:p.Leu1485=