Canonical Allele Identifier: CA1239490454

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742413_25742416delinsAAGG , CM000664.2:g.25742413_25742416delinsAAGG	GRCh38
NC_000002.11:g.25965282_25965285delinsAAGG , CM000664.1:g.25965282_25965285delinsAAGG	GRCh37
NC_000002.10:g.25818786_25818789delinsAAGG	NCBI36
NG_052995.1:g.141101_141104delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3918_3921delinsCCTT	ENSP00000337250.5:p.Leu1306=
ENST00000435504.9:c.3921_3924delinsCCTT MANE Select	ENSP00000391447.3:p.Leu1307=
ENST00000336112.8:c.3837_3840delinsCCTT	ENSP00000337250.4:p.Leu1279=
ENST00000404843.5:c.2370_2373delinsCCTT	ENSP00000383920.1:p.Leu790=
ENST00000435504.8:c.3921_3924delinsCCTT	ENSP00000391447.3:p.Leu1307=
NM_018263.4:c.3921_3924delinsCCTT	NP_060733.4:p.Leu1307=
XM_006712039.2:c.3555_3558delinsCCTT	XP_006712102.1:p.Leu1185=
XM_006712040.1:c.3141_3144delinsCCTT	XP_006712103.1:p.Leu1047=
XM_011532950.1:c.3918_3921delinsCCTT	XP_011531252.1:p.Leu1306=
XM_011532951.1:c.3747_3750delinsCCTT	XP_011531253.1:p.Leu1249=
NM_018263.5:c.3921_3924delinsCCTT	NP_060733.4:p.Leu1307=
XM_006712039.3:c.3555_3558delinsCCTT	XP_006712102.1:p.Leu1185=
XM_006712040.2:c.3141_3144delinsCCTT	XP_006712103.1:p.Leu1047=
XM_011532950.3:c.3918_3921delinsCCTT	XP_011531252.1:p.Leu1306=
XM_011532951.2:c.3747_3750delinsCCTT	XP_011531253.1:p.Leu1249=
XM_017004430.1:c.3141_3144delinsCCTT	XP_016859919.1:p.Leu1047=
XM_024452974.1:c.4101_4104delinsCCTT	XP_024308742.1:p.Leu1367=
NM_001369346.1:c.3747_3750delinsCCTT	NP_001356275.1:p.Leu1249=
NM_001369347.1:c.3141_3144delinsCCTT	NP_001356276.1:p.Leu1047=
NM_018263.6:c.3921_3924delinsCCTT MANE Select	NP_060733.4:p.Leu1307=