Canonical Allele Identifier: CA2294857970

Gene: ASXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.33744056_33744058delinsTCA , CM000680.2:g.33744056_33744058delinsTCA	GRCh38
NC_000018.9:g.31324020_31324022delinsTCA , CM000680.1:g.31324020_31324022delinsTCA	GRCh37
NC_000018.8:g.29578018_29578020delinsTCA	NCBI36
NG_055244.1:g.170480_170482delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696964.1:c.4211_4213delinsTCA	ENSP00000513003.1:p.Val1404=
ENST00000269197.12:c.4208_4210delinsTCA MANE Select	ENSP00000269197.4:p.Val1403=
ENST00000681521.1:c.4088_4090delinsTCA	ENSP00000506037.1:p.Val1363=
ENST00000269197.9:c.4208_4210delinsTCA	ENSP00000269197.4:p.Val1403=
NM_030632.1:c.4208_4210delinsTCA	NP_085135.1:p.Val1403=
XM_005258356.1:c.4211_4213delinsTCA	XP_005258413.1:p.Val1404=
XM_011526205.1:c.4184_4186delinsTCA	XP_011524507.1:p.Val1395=
XM_011526206.1:c.4130_4132delinsTCA	XP_011524508.1:p.Val1377=
XM_011526207.1:c.4130_4132delinsTCA	XP_011524509.1:p.Val1377=
XM_011526208.1:c.4091_4093delinsTCA	XP_011524510.1:p.Val1364=
XM_011526209.1:c.4040_4042delinsTCA	XP_011524511.1:p.Val1347=
XM_011526210.1:c.4040_4042delinsTCA	XP_011524512.1:p.Val1347=
XM_011526211.1:c.4040_4042delinsTCA	XP_011524513.1:p.Val1347=
XM_011526212.1:c.4040_4042delinsTCA	XP_011524514.1:p.Val1347=
XM_011526213.1:c.4040_4042delinsTCA	XP_011524515.1:p.Val1347=
XM_011526214.1:c.4040_4042delinsTCA	XP_011524516.1:p.Val1347=
XM_011526215.1:c.1172_1174delinsTCA	XP_011524517.1:p.Val391=
NM_030632.2:c.4208_4210delinsTCA	NP_085135.1:p.Val1403=
XM_011526205.2:c.4184_4186delinsTCA	XP_011524507.1:p.Val1395=
XM_011526206.2:c.4130_4132delinsTCA	XP_011524508.1:p.Val1377=
XM_011526213.2:c.4040_4042delinsTCA	XP_011524515.1:p.Val1347=
XM_017026012.1:c.4130_4132delinsTCA	XP_016881501.1:p.Val1377=
XM_017026013.1:c.4040_4042delinsTCA	XP_016881502.1:p.Val1347=
XM_017026014.2:c.4040_4042delinsTCA	XP_016881503.1:p.Val1347=
XM_024451269.1:c.4040_4042delinsTCA	XP_024307037.1:p.Val1347=
NM_030632.3:c.4208_4210delinsTCA MANE Select	NP_085135.1:p.Val1403=