Canonical Allele Identifier: CA2294857603

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33743208_33743220delinsCTTCCAGACCTCT , CM000680.2:g.33743208_33743220delinsCTTCCAGACCTCT	GRCh38
NC_000018.9:g.31323172_31323184delinsCTTCCAGACCTCT , CM000680.1:g.31323172_31323184delinsCTTCCAGACCTCT	GRCh37
NC_000018.8:g.29577170_29577182delinsCTTCCAGACCTCT	NCBI36
NG_055244.1:g.169632_169644delinsCTTCCAGACCTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.3363_3375delinsCTTCCAGACCTCT	ENSP00000513003.1:p.Leu1121=
ENST00000269197.12:c.3360_3372delinsCTTCCAGACCTCT MANE Select	ENSP00000269197.4:p.Leu1120=
ENST00000592288.6:c.*2484_*2496delinsCTTCCAGACCTCT	ENSP00000465053.1:n.*2484_*2496delinsCTTC...
ENST00000592541.6:c.*3019_*3031delinsCTTCCAGACCTCT	ENSP00000466655.2:n.*3019_*3031delinsCTTC...
ENST00000593195.6:c.3572_3584delinsCTTCCAGACCTCT	ENSP00000466073.1:n.3572_3584delinsCTTCCA...
ENST00000642541.1:c.3192_3204delinsCTTCCAGACCTCT	ENSP00000493665.1:p.Leu1064=
ENST00000681521.1:c.3240_3252delinsCTTCCAGACCTCT	ENSP00000506037.1:p.Leu1080=
ENST00000269197.9:c.3360_3372delinsCTTCCAGACCTCT	ENSP00000269197.4:p.Leu1120=
ENST00000592288.5:c.*2484_*2496delinsCTTCCAGACCTCT	ENSP00000465053.1:n.*2484_*2496delinsCTTC...
NM_030632.1:c.3360_3372delinsCTTCCAGACCTCT	NP_085135.1:p.Leu1120=
XM_005258356.1:c.3363_3375delinsCTTCCAGACCTCT	XP_005258413.1:p.Leu1121=
XM_011526205.1:c.3336_3348delinsCTTCCAGACCTCT	XP_011524507.1:p.Leu1112=
XM_011526206.1:c.3282_3294delinsCTTCCAGACCTCT	XP_011524508.1:p.Leu1094=
XM_011526207.1:c.3282_3294delinsCTTCCAGACCTCT	XP_011524509.1:p.Leu1094=
XM_011526208.1:c.3243_3255delinsCTTCCAGACCTCT	XP_011524510.1:p.Leu1081=
XM_011526209.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524511.1:p.Leu1064=
XM_011526210.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524512.1:p.Leu1064=
XM_011526211.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524513.1:p.Leu1064=
XM_011526212.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524514.1:p.Leu1064=
XM_011526213.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524515.1:p.Leu1064=
XM_011526214.1:c.3192_3204delinsCTTCCAGACCTCT	XP_011524516.1:p.Leu1064=
XM_011526215.1:c.324_336delinsCTTCCAGACCTCT	XP_011524517.1:p.Leu108=
NM_030632.2:c.3360_3372delinsCTTCCAGACCTCT	NP_085135.1:p.Leu1120=
XM_011526205.2:c.3336_3348delinsCTTCCAGACCTCT	XP_011524507.1:p.Leu1112=
XM_011526206.2:c.3282_3294delinsCTTCCAGACCTCT	XP_011524508.1:p.Leu1094=
XM_011526213.2:c.3192_3204delinsCTTCCAGACCTCT	XP_011524515.1:p.Leu1064=
XM_017026012.1:c.3282_3294delinsCTTCCAGACCTCT	XP_016881501.1:p.Leu1094=
XM_017026013.1:c.3192_3204delinsCTTCCAGACCTCT	XP_016881502.1:p.Leu1064=
XM_017026014.2:c.3192_3204delinsCTTCCAGACCTCT	XP_016881503.1:p.Leu1064=
XM_024451269.1:c.3192_3204delinsCTTCCAGACCTCT	XP_024307037.1:p.Leu1064=
NM_030632.3:c.3360_3372delinsCTTCCAGACCTCT MANE Select	NP_085135.1:p.Leu1120=