Canonical Allele Identifier: CA425353720

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742542-T-C
• MyVariant Identifiers: chr2:g.25965411T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742542T>C , CM000664.2:g.25742542T>C	GRCh38
NC_000002.11:g.25965411T>C , CM000664.1:g.25965411T>C	GRCh37
NC_000002.10:g.25818915T>C	NCBI36
NG_052995.1:g.140975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3792A>G	ENSP00000337250.5:p.Leu1264=
ENST00000435504.9:c.3795A>G MANE Select	ENSP00000391447.3:p.Leu1265=
ENST00000336112.8:c.3711A>G	ENSP00000337250.4:p.Leu1237=
ENST00000404843.5:c.2244A>G	ENSP00000383920.1:p.Leu748=
ENST00000435504.8:c.3795A>G	ENSP00000391447.3:p.Leu1265=
NM_018263.4:c.3795A>G	NP_060733.4:p.Leu1265=
XM_006712039.2:c.3429A>G	XP_006712102.1:p.Leu1143=
XM_006712040.1:c.3015A>G	XP_006712103.1:p.Leu1005=
XM_011532950.1:c.3792A>G	XP_011531252.1:p.Leu1264=
XM_011532951.1:c.3621A>G	XP_011531253.1:p.Leu1207=
NM_018263.5:c.3795A>G	NP_060733.4:p.Leu1265=
XM_006712039.3:c.3429A>G	XP_006712102.1:p.Leu1143=
XM_006712040.2:c.3015A>G	XP_006712103.1:p.Leu1005=
XM_011532950.3:c.3792A>G	XP_011531252.1:p.Leu1264=
XM_011532951.2:c.3621A>G	XP_011531253.1:p.Leu1207=
XM_017004430.1:c.3015A>G	XP_016859919.1:p.Leu1005=
XM_024452974.1:c.3975A>G	XP_024308742.1:p.Leu1325=
NM_001369346.1:c.3621A>G	NP_001356275.1:p.Leu1207=
NM_001369347.1:c.3015A>G	NP_001356276.1:p.Leu1005=
NM_018263.6:c.3795A>G MANE Select	NP_060733.4:p.Leu1265=