Canonical Allele Identifier: CA1239490386

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742276A= , CM000664.2:g.25742276A=	GRCh38
NC_000002.11:g.25965145A= , CM000664.1:g.25965145A=	GRCh37
NC_000002.10:g.25818649A=	NCBI36
NG_052995.1:g.141241T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4058T=	ENSP00000337250.5:p.Val1353=
ENST00000435504.9:c.4061T= MANE Select	ENSP00000391447.3:p.Val1354=
ENST00000336112.8:c.3977T=	ENSP00000337250.4:p.Val1326=
ENST00000404843.5:c.2510T=	ENSP00000383920.1:p.Val837=
ENST00000435504.8:c.4061T=	ENSP00000391447.3:p.Val1354=
NM_018263.4:c.4061T=	NP_060733.4:p.Val1354=
XM_006712039.2:c.3695T=	XP_006712102.1:p.Val1232=
XM_006712040.1:c.3281T=	XP_006712103.1:p.Val1094=
XM_011532950.1:c.4058T=	XP_011531252.1:p.Val1353=
XM_011532951.1:c.3887T=	XP_011531253.1:p.Val1296=
NM_018263.5:c.4061T=	NP_060733.4:p.Val1354=
XM_006712039.3:c.3695T=	XP_006712102.1:p.Val1232=
XM_006712040.2:c.3281T=	XP_006712103.1:p.Val1094=
XM_011532950.3:c.4058T=	XP_011531252.1:p.Val1353=
XM_011532951.2:c.3887T=	XP_011531253.1:p.Val1296=
XM_017004430.1:c.3281T=	XP_016859919.1:p.Val1094=
XM_024452974.1:c.4241T=	XP_024308742.1:p.Val1414=
NM_001369346.1:c.3887T=	NP_001356275.1:p.Val1296=
NM_001369347.1:c.3281T=	NP_001356276.1:p.Val1094=
NM_018263.6:c.4061T= MANE Select	NP_060733.4:p.Val1354=