Canonical Allele Identifier: CA1239490455

Gene: ASXL2

Linked Data

• dbSNP Id: rs2087846348

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742416_25742418del , CM000664.2:g.25742416_25742418del	GRCh38
NC_000002.11:g.25965285_25965287del , CM000664.1:g.25965285_25965287del	GRCh37
NC_000002.10:g.25818789_25818791del	NCBI36
NG_052995.1:g.141101_141103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3918_3920del	ENSP00000337250.5:p.Leu1307del
ENST00000435504.9:c.3921_3923del MANE Select	ENSP00000391447.3:p.Leu1308del
ENST00000336112.8:c.3837_3839del	ENSP00000337250.4:p.Leu1280del
ENST00000404843.5:c.2370_2372del	ENSP00000383920.1:p.Leu791del
ENST00000435504.8:c.3921_3923del	ENSP00000391447.3:p.Leu1308del
NM_018263.4:c.3921_3923del	NP_060733.4:p.Leu1308del
XM_006712039.2:c.3555_3557del	XP_006712102.1:p.Leu1186del
XM_006712040.1:c.3141_3143del	XP_006712103.1:p.Leu1048del
XM_011532950.1:c.3918_3920del	XP_011531252.1:p.Leu1307del
XM_011532951.1:c.3747_3749del	XP_011531253.1:p.Leu1250del
NM_018263.5:c.3921_3923del	NP_060733.4:p.Leu1308del
XM_006712039.3:c.3555_3557del	XP_006712102.1:p.Leu1186del
XM_006712040.2:c.3141_3143del	XP_006712103.1:p.Leu1048del
XM_011532950.3:c.3918_3920del	XP_011531252.1:p.Leu1307del
XM_011532951.2:c.3747_3749del	XP_011531253.1:p.Leu1250del
XM_017004430.1:c.3141_3143del	XP_016859919.1:p.Leu1048del
XM_024452974.1:c.4101_4103del	XP_024308742.1:p.Leu1368del
NM_001369346.1:c.3747_3749del	NP_001356275.1:p.Leu1250del
NM_001369347.1:c.3141_3143del	NP_001356276.1:p.Leu1048del
NM_018263.6:c.3921_3923del MANE Select	NP_060733.4:p.Leu1308del