Canonical Allele Identifier: CA425353728

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965423T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742554T>A , CM000664.2:g.25742554T>A	GRCh38
NC_000002.11:g.25965423T>A , CM000664.1:g.25965423T>A	GRCh37
NC_000002.10:g.25818927T>A	NCBI36
NG_052995.1:g.140963A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3780A>T	ENSP00000337250.5:p.Leu1260=
ENST00000435504.9:c.3783A>T MANE Select	ENSP00000391447.3:p.Leu1261=
ENST00000336112.8:c.3699A>T	ENSP00000337250.4:p.Leu1233=
ENST00000404843.5:c.2232A>T	ENSP00000383920.1:p.Leu744=
ENST00000435504.8:c.3783A>T	ENSP00000391447.3:p.Leu1261=
NM_018263.4:c.3783A>T	NP_060733.4:p.Leu1261=
XM_006712039.2:c.3417A>T	XP_006712102.1:p.Leu1139=
XM_006712040.1:c.3003A>T	XP_006712103.1:p.Leu1001=
XM_011532950.1:c.3780A>T	XP_011531252.1:p.Leu1260=
XM_011532951.1:c.3609A>T	XP_011531253.1:p.Leu1203=
NM_018263.5:c.3783A>T	NP_060733.4:p.Leu1261=
XM_006712039.3:c.3417A>T	XP_006712102.1:p.Leu1139=
XM_006712040.2:c.3003A>T	XP_006712103.1:p.Leu1001=
XM_011532950.3:c.3780A>T	XP_011531252.1:p.Leu1260=
XM_011532951.2:c.3609A>T	XP_011531253.1:p.Leu1203=
XM_017004430.1:c.3003A>T	XP_016859919.1:p.Leu1001=
XM_024452974.1:c.3963A>T	XP_024308742.1:p.Leu1321=
NM_001369346.1:c.3609A>T	NP_001356275.1:p.Leu1203=
NM_001369347.1:c.3003A>T	NP_001356276.1:p.Leu1001=
NM_018263.6:c.3783A>T MANE Select	NP_060733.4:p.Leu1261=