Canonical Allele Identifier: CA425353695

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965363T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742494T>C , CM000664.2:g.25742494T>C	GRCh38
NC_000002.11:g.25965363T>C , CM000664.1:g.25965363T>C	GRCh37
NC_000002.10:g.25818867T>C	NCBI36
NG_052995.1:g.141023A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3840A>G	ENSP00000337250.5:p.Ala1280=
ENST00000435504.9:c.3843A>G MANE Select	ENSP00000391447.3:p.Ala1281=
ENST00000336112.8:c.3759A>G	ENSP00000337250.4:p.Ala1253=
ENST00000404843.5:c.2292A>G	ENSP00000383920.1:p.Ala764=
ENST00000435504.8:c.3843A>G	ENSP00000391447.3:p.Ala1281=
NM_018263.4:c.3843A>G	NP_060733.4:p.Ala1281=
XM_006712039.2:c.3477A>G	XP_006712102.1:p.Ala1159=
XM_006712040.1:c.3063A>G	XP_006712103.1:p.Ala1021=
XM_011532950.1:c.3840A>G	XP_011531252.1:p.Ala1280=
XM_011532951.1:c.3669A>G	XP_011531253.1:p.Ala1223=
NM_018263.5:c.3843A>G	NP_060733.4:p.Ala1281=
XM_006712039.3:c.3477A>G	XP_006712102.1:p.Ala1159=
XM_006712040.2:c.3063A>G	XP_006712103.1:p.Ala1021=
XM_011532950.3:c.3840A>G	XP_011531252.1:p.Ala1280=
XM_011532951.2:c.3669A>G	XP_011531253.1:p.Ala1223=
XM_017004430.1:c.3063A>G	XP_016859919.1:p.Ala1021=
XM_024452974.1:c.4023A>G	XP_024308742.1:p.Ala1341=
NM_001369346.1:c.3669A>G	NP_001356275.1:p.Ala1223=
NM_001369347.1:c.3063A>G	NP_001356276.1:p.Ala1021=
NM_018263.6:c.3843A>G MANE Select	NP_060733.4:p.Ala1281=