Canonical Allele Identifier: CA425354988

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965333A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742464A>C , CM000664.2:g.25742464A>C	GRCh38
NC_000002.11:g.25965333A>C , CM000664.1:g.25965333A>C	GRCh37
NC_000002.10:g.25818837A>C	NCBI36
NG_052995.1:g.141053T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3870T>G	ENSP00000337250.5:p.Ser1290=
ENST00000435504.9:c.3873T>G MANE Select	ENSP00000391447.3:p.Ser1291=
ENST00000336112.8:c.3789T>G	ENSP00000337250.4:p.Ser1263=
ENST00000404843.5:c.2322T>G	ENSP00000383920.1:p.Ser774=
ENST00000435504.8:c.3873T>G	ENSP00000391447.3:p.Ser1291=
NM_018263.4:c.3873T>G	NP_060733.4:p.Ser1291=
XM_006712039.2:c.3507T>G	XP_006712102.1:p.Ser1169=
XM_006712040.1:c.3093T>G	XP_006712103.1:p.Ser1031=
XM_011532950.1:c.3870T>G	XP_011531252.1:p.Ser1290=
XM_011532951.1:c.3699T>G	XP_011531253.1:p.Ser1233=
NM_018263.5:c.3873T>G	NP_060733.4:p.Ser1291=
XM_006712039.3:c.3507T>G	XP_006712102.1:p.Ser1169=
XM_006712040.2:c.3093T>G	XP_006712103.1:p.Ser1031=
XM_011532950.3:c.3870T>G	XP_011531252.1:p.Ser1290=
XM_011532951.2:c.3699T>G	XP_011531253.1:p.Ser1233=
XM_017004430.1:c.3093T>G	XP_016859919.1:p.Ser1031=
XM_024452974.1:c.4053T>G	XP_024308742.1:p.Ser1351=
NM_001369346.1:c.3699T>G	NP_001356275.1:p.Ser1233=
NM_001369347.1:c.3093T>G	NP_001356276.1:p.Ser1031=
NM_018263.6:c.3873T>G MANE Select	NP_060733.4:p.Ser1291=