Canonical Allele Identifier: CA1239490310

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742053_25742055delinsGCA , CM000664.2:g.25742053_25742055delinsGCA	GRCh38
NC_000002.11:g.25964922_25964924delinsGCA , CM000664.1:g.25964922_25964924delinsGCA	GRCh37
NC_000002.10:g.25818426_25818428delinsGCA	NCBI36
NG_052995.1:g.141462_141464delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4279_4281delinsTGC	ENSP00000337250.5:p.Cys1427=
ENST00000435504.9:c.4282_4284delinsTGC MANE Select	ENSP00000391447.3:p.Cys1428=
ENST00000336112.8:c.4198_4200delinsTGC	ENSP00000337250.4:p.Cys1400=
ENST00000404843.5:c.2731_2733delinsTGC	ENSP00000383920.1:p.Cys911=
ENST00000435504.8:c.4282_4284delinsTGC	ENSP00000391447.3:p.Cys1428=
NM_018263.4:c.4282_4284delinsTGC	NP_060733.4:p.Cys1428=
XM_006712039.2:c.3916_3918delinsTGC	XP_006712102.1:p.Cys1306=
XM_006712040.1:c.3502_3504delinsTGC	XP_006712103.1:p.Cys1168=
XM_011532950.1:c.4279_4281delinsTGC	XP_011531252.1:p.Cys1427=
XM_011532951.1:c.4108_4110delinsTGC	XP_011531253.1:p.Cys1370=
NM_018263.5:c.4282_4284delinsTGC	NP_060733.4:p.Cys1428=
XM_006712039.3:c.3916_3918delinsTGC	XP_006712102.1:p.Cys1306=
XM_006712040.2:c.3502_3504delinsTGC	XP_006712103.1:p.Cys1168=
XM_011532950.3:c.4279_4281delinsTGC	XP_011531252.1:p.Cys1427=
XM_011532951.2:c.4108_4110delinsTGC	XP_011531253.1:p.Cys1370=
XM_017004430.1:c.3502_3504delinsTGC	XP_016859919.1:p.Cys1168=
XM_024452974.1:c.4462_4464delinsTGC	XP_024308742.1:p.Cys1488=
NM_001369346.1:c.4108_4110delinsTGC	NP_001356275.1:p.Cys1370=
NM_001369347.1:c.3502_3504delinsTGC	NP_001356276.1:p.Cys1168=
NM_018263.6:c.4282_4284delinsTGC MANE Select	NP_060733.4:p.Cys1428=