Canonical Allele Identifier: CA2294858047

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744219_33744220delinsAG , CM000680.2:g.33744219_33744220delinsAG	GRCh38
NC_000018.9:g.31324183_31324184delinsAG , CM000680.1:g.31324183_31324184delinsAG	GRCh37
NC_000018.8:g.29578181_29578182delinsAG	NCBI36
NG_055244.1:g.170643_170644delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696964.1:c.4374_4375delinsAG	ENSP00000513003.1:p.Pro1458=
ENST00000269197.12:c.4371_4372delinsAG MANE Select	ENSP00000269197.4:p.Pro1457=
ENST00000681521.1:c.4251_4252delinsAG	ENSP00000506037.1:p.Pro1417=
ENST00000269197.9:c.4371_4372delinsAG	ENSP00000269197.4:p.Pro1457=
NM_030632.1:c.4371_4372delinsAG	NP_085135.1:p.Pro1457=
XM_005258356.1:c.4374_4375delinsAG	XP_005258413.1:p.Pro1458=
XM_011526205.1:c.4347_4348delinsAG	XP_011524507.1:p.Pro1449=
XM_011526206.1:c.4293_4294delinsAG	XP_011524508.1:p.Pro1431=
XM_011526207.1:c.4293_4294delinsAG	XP_011524509.1:p.Pro1431=
XM_011526208.1:c.4254_4255delinsAG	XP_011524510.1:p.Pro1418=
XM_011526209.1:c.4203_4204delinsAG	XP_011524511.1:p.Pro1401=
XM_011526210.1:c.4203_4204delinsAG	XP_011524512.1:p.Pro1401=
XM_011526211.1:c.4203_4204delinsAG	XP_011524513.1:p.Pro1401=
XM_011526212.1:c.4203_4204delinsAG	XP_011524514.1:p.Pro1401=
XM_011526213.1:c.4203_4204delinsAG	XP_011524515.1:p.Pro1401=
XM_011526214.1:c.4203_4204delinsAG	XP_011524516.1:p.Pro1401=
XM_011526215.1:c.1335_1336delinsAG	XP_011524517.1:p.Pro445=
NM_030632.2:c.4371_4372delinsAG	NP_085135.1:p.Pro1457=
XM_011526205.2:c.4347_4348delinsAG	XP_011524507.1:p.Pro1449=
XM_011526206.2:c.4293_4294delinsAG	XP_011524508.1:p.Pro1431=
XM_011526213.2:c.4203_4204delinsAG	XP_011524515.1:p.Pro1401=
XM_017026012.1:c.4293_4294delinsAG	XP_016881501.1:p.Pro1431=
XM_017026013.1:c.4203_4204delinsAG	XP_016881502.1:p.Pro1401=
XM_017026014.2:c.4203_4204delinsAG	XP_016881503.1:p.Pro1401=
XM_024451269.1:c.4203_4204delinsAG	XP_024307037.1:p.Pro1401=
NM_030632.3:c.4371_4372delinsAG MANE Select	NP_085135.1:p.Pro1457=