Canonical Allele Identifier: CA1239490404

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742312T= , CM000664.2:g.25742312T=	GRCh38
NC_000002.11:g.25965181T= , CM000664.1:g.25965181T=	GRCh37
NC_000002.10:g.25818685T=	NCBI36
NG_052995.1:g.141205A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4022A=	ENSP00000337250.5:p.Asn1341=
ENST00000435504.9:c.4025A= MANE Select	ENSP00000391447.3:p.Asn1342=
ENST00000336112.8:c.3941A=	ENSP00000337250.4:p.Asn1314=
ENST00000404843.5:c.2474A=	ENSP00000383920.1:p.Asn825=
ENST00000435504.8:c.4025A=	ENSP00000391447.3:p.Asn1342=
NM_018263.4:c.4025A=	NP_060733.4:p.Asn1342=
XM_006712039.2:c.3659A=	XP_006712102.1:p.Asn1220=
XM_006712040.1:c.3245A=	XP_006712103.1:p.Asn1082=
XM_011532950.1:c.4022A=	XP_011531252.1:p.Asn1341=
XM_011532951.1:c.3851A=	XP_011531253.1:p.Asn1284=
NM_018263.5:c.4025A=	NP_060733.4:p.Asn1342=
XM_006712039.3:c.3659A=	XP_006712102.1:p.Asn1220=
XM_006712040.2:c.3245A=	XP_006712103.1:p.Asn1082=
XM_011532950.3:c.4022A=	XP_011531252.1:p.Asn1341=
XM_011532951.2:c.3851A=	XP_011531253.1:p.Asn1284=
XM_017004430.1:c.3245A=	XP_016859919.1:p.Asn1082=
XM_024452974.1:c.4205A=	XP_024308742.1:p.Asn1402=
NM_001369346.1:c.3851A=	NP_001356275.1:p.Asn1284=
NM_001369347.1:c.3245A=	NP_001356276.1:p.Asn1082=
NM_018263.6:c.4025A= MANE Select	NP_060733.4:p.Asn1342=