Canonical Allele Identifier: CA425181256

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964931G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742062G>C , CM000664.2:g.25742062G>C	GRCh38
NC_000002.11:g.25964931G>C , CM000664.1:g.25964931G>C	GRCh37
NC_000002.10:g.25818435G>C	NCBI36
NG_052995.1:g.141455C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4272C>G	ENSP00000337250.5:p.Ser1424=
ENST00000435504.9:c.4275C>G MANE Select	ENSP00000391447.3:p.Ser1425=
ENST00000336112.8:c.4191C>G	ENSP00000337250.4:p.Ser1397=
ENST00000404843.5:c.2724C>G	ENSP00000383920.1:p.Ser908=
ENST00000435504.8:c.4275C>G	ENSP00000391447.3:p.Ser1425=
NM_018263.4:c.4275C>G	NP_060733.4:p.Ser1425=
XM_006712039.2:c.3909C>G	XP_006712102.1:p.Ser1303=
XM_006712040.1:c.3495C>G	XP_006712103.1:p.Ser1165=
XM_011532950.1:c.4272C>G	XP_011531252.1:p.Ser1424=
XM_011532951.1:c.4101C>G	XP_011531253.1:p.Ser1367=
NM_018263.5:c.4275C>G	NP_060733.4:p.Ser1425=
XM_006712039.3:c.3909C>G	XP_006712102.1:p.Ser1303=
XM_006712040.2:c.3495C>G	XP_006712103.1:p.Ser1165=
XM_011532950.3:c.4272C>G	XP_011531252.1:p.Ser1424=
XM_011532951.2:c.4101C>G	XP_011531253.1:p.Ser1367=
XM_017004430.1:c.3495C>G	XP_016859919.1:p.Ser1165=
XM_024452974.1:c.4455C>G	XP_024308742.1:p.Ser1485=
NM_001369346.1:c.4101C>G	NP_001356275.1:p.Ser1367=
NM_001369347.1:c.3495C>G	NP_001356276.1:p.Ser1165=
NM_018263.6:c.4275C>G MANE Select	NP_060733.4:p.Ser1425=