Canonical Allele Identifier: CA1239490400

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742307_25742309delinsCAG , CM000664.2:g.25742307_25742309delinsCAG	GRCh38
NC_000002.11:g.25965176_25965178delinsCAG , CM000664.1:g.25965176_25965178delinsCAG	GRCh37
NC_000002.10:g.25818680_25818682delinsCAG	NCBI36
NG_052995.1:g.141208_141210delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4025_4027delinsCTG	ENSP00000337250.5:p.Ser1342=
ENST00000435504.9:c.4028_4030delinsCTG MANE Select	ENSP00000391447.3:p.Ser1343=
ENST00000336112.8:c.3944_3946delinsCTG	ENSP00000337250.4:p.Ser1315=
ENST00000404843.5:c.2477_2479delinsCTG	ENSP00000383920.1:p.Ser826=
ENST00000435504.8:c.4028_4030delinsCTG	ENSP00000391447.3:p.Ser1343=
NM_018263.4:c.4028_4030delinsCTG	NP_060733.4:p.Ser1343=
XM_006712039.2:c.3662_3664delinsCTG	XP_006712102.1:p.Ser1221=
XM_006712040.1:c.3248_3250delinsCTG	XP_006712103.1:p.Ser1083=
XM_011532950.1:c.4025_4027delinsCTG	XP_011531252.1:p.Ser1342=
XM_011532951.1:c.3854_3856delinsCTG	XP_011531253.1:p.Ser1285=
NM_018263.5:c.4028_4030delinsCTG	NP_060733.4:p.Ser1343=
XM_006712039.3:c.3662_3664delinsCTG	XP_006712102.1:p.Ser1221=
XM_006712040.2:c.3248_3250delinsCTG	XP_006712103.1:p.Ser1083=
XM_011532950.3:c.4025_4027delinsCTG	XP_011531252.1:p.Ser1342=
XM_011532951.2:c.3854_3856delinsCTG	XP_011531253.1:p.Ser1285=
XM_017004430.1:c.3248_3250delinsCTG	XP_016859919.1:p.Ser1083=
XM_024452974.1:c.4208_4210delinsCTG	XP_024308742.1:p.Ser1403=
NM_001369346.1:c.3854_3856delinsCTG	NP_001356275.1:p.Ser1285=
NM_001369347.1:c.3248_3250delinsCTG	NP_001356276.1:p.Ser1083=
NM_018263.6:c.4028_4030delinsCTG MANE Select	NP_060733.4:p.Ser1343=