Canonical Allele Identifier: CA1239490494

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742483_25742484delinsCT , CM000664.2:g.25742483_25742484delinsCT	GRCh38
NC_000002.11:g.25965352_25965353delinsCT , CM000664.1:g.25965352_25965353delinsCT	GRCh37
NC_000002.10:g.25818856_25818857delinsCT	NCBI36
NG_052995.1:g.141033_141034delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3850_3851delinsAG	ENSP00000337250.5:p.Ser1284=
ENST00000435504.9:c.3853_3854delinsAG MANE Select	ENSP00000391447.3:p.Ser1285=
ENST00000336112.8:c.3769_3770delinsAG	ENSP00000337250.4:p.Ser1257=
ENST00000404843.5:c.2302_2303delinsAG	ENSP00000383920.1:p.Ser768=
ENST00000435504.8:c.3853_3854delinsAG	ENSP00000391447.3:p.Ser1285=
NM_018263.4:c.3853_3854delinsAG	NP_060733.4:p.Ser1285=
XM_006712039.2:c.3487_3488delinsAG	XP_006712102.1:p.Ser1163=
XM_006712040.1:c.3073_3074delinsAG	XP_006712103.1:p.Ser1025=
XM_011532950.1:c.3850_3851delinsAG	XP_011531252.1:p.Ser1284=
XM_011532951.1:c.3679_3680delinsAG	XP_011531253.1:p.Ser1227=
NM_018263.5:c.3853_3854delinsAG	NP_060733.4:p.Ser1285=
XM_006712039.3:c.3487_3488delinsAG	XP_006712102.1:p.Ser1163=
XM_006712040.2:c.3073_3074delinsAG	XP_006712103.1:p.Ser1025=
XM_011532950.3:c.3850_3851delinsAG	XP_011531252.1:p.Ser1284=
XM_011532951.2:c.3679_3680delinsAG	XP_011531253.1:p.Ser1227=
XM_017004430.1:c.3073_3074delinsAG	XP_016859919.1:p.Ser1025=
XM_024452974.1:c.4033_4034delinsAG	XP_024308742.1:p.Ser1345=
NM_001369346.1:c.3679_3680delinsAG	NP_001356275.1:p.Ser1227=
NM_001369347.1:c.3073_3074delinsAG	NP_001356276.1:p.Ser1025=
NM_018263.6:c.3853_3854delinsAG MANE Select	NP_060733.4:p.Ser1285=