Canonical Allele Identifier: CA425181305

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964988G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742119G>A , CM000664.2:g.25742119G>A	GRCh38
NC_000002.11:g.25964988G>A , CM000664.1:g.25964988G>A	GRCh37
NC_000002.10:g.25818492G>A	NCBI36
NG_052995.1:g.141398C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4215C>T	ENSP00000337250.5:p.Ala1405=
ENST00000435504.9:c.4218C>T MANE Select	ENSP00000391447.3:p.Ala1406=
ENST00000336112.8:c.4134C>T	ENSP00000337250.4:p.Ala1378=
ENST00000404843.5:c.2667C>T	ENSP00000383920.1:p.Ala889=
ENST00000435504.8:c.4218C>T	ENSP00000391447.3:p.Ala1406=
NM_018263.4:c.4218C>T	NP_060733.4:p.Ala1406=
XM_006712039.2:c.3852C>T	XP_006712102.1:p.Ala1284=
XM_006712040.1:c.3438C>T	XP_006712103.1:p.Ala1146=
XM_011532950.1:c.4215C>T	XP_011531252.1:p.Ala1405=
XM_011532951.1:c.4044C>T	XP_011531253.1:p.Ala1348=
NM_018263.5:c.4218C>T	NP_060733.4:p.Ala1406=
XM_006712039.3:c.3852C>T	XP_006712102.1:p.Ala1284=
XM_006712040.2:c.3438C>T	XP_006712103.1:p.Ala1146=
XM_011532950.3:c.4215C>T	XP_011531252.1:p.Ala1405=
XM_011532951.2:c.4044C>T	XP_011531253.1:p.Ala1348=
XM_017004430.1:c.3438C>T	XP_016859919.1:p.Ala1146=
XM_024452974.1:c.4398C>T	XP_024308742.1:p.Ala1466=
NM_001369346.1:c.4044C>T	NP_001356275.1:p.Ala1348=
NM_001369347.1:c.3438C>T	NP_001356276.1:p.Ala1146=
NM_018263.6:c.4218C>T MANE Select	NP_060733.4:p.Ala1406=