Canonical Allele Identifier: CA425181235

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25964901C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742032C>T , CM000664.2:g.25742032C>T	GRCh38
NC_000002.11:g.25964901C>T , CM000664.1:g.25964901C>T	GRCh37
NC_000002.10:g.25818405C>T	NCBI36
NG_052995.1:g.141485G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4302G>A	ENSP00000337250.5:p.Arg1434=
ENST00000435504.9:c.4305G>A MANE Select	ENSP00000391447.3:p.Arg1435=
ENST00000336112.8:c.4221G>A	ENSP00000337250.4:p.Arg1407=
ENST00000404843.5:c.2754G>A	ENSP00000383920.1:p.Arg918=
ENST00000435504.8:c.4305G>A	ENSP00000391447.3:p.Arg1435=
NM_018263.4:c.4305G>A	NP_060733.4:p.Arg1435=
XM_006712039.2:c.3939G>A	XP_006712102.1:p.Arg1313=
XM_006712040.1:c.3525G>A	XP_006712103.1:p.Arg1175=
XM_011532950.1:c.4302G>A	XP_011531252.1:p.Arg1434=
XM_011532951.1:c.4131G>A	XP_011531253.1:p.Arg1377=
NM_018263.5:c.4305G>A	NP_060733.4:p.Arg1435=
XM_006712039.3:c.3939G>A	XP_006712102.1:p.Arg1313=
XM_006712040.2:c.3525G>A	XP_006712103.1:p.Arg1175=
XM_011532950.3:c.4302G>A	XP_011531252.1:p.Arg1434=
XM_011532951.2:c.4131G>A	XP_011531253.1:p.Arg1377=
XM_017004430.1:c.3525G>A	XP_016859919.1:p.Arg1175=
XM_024452974.1:c.4485G>A	XP_024308742.1:p.Arg1495=
NM_001369346.1:c.4131G>A	NP_001356275.1:p.Arg1377=
NM_001369347.1:c.3525G>A	NP_001356276.1:p.Arg1175=
NM_018263.6:c.4305G>A MANE Select	NP_060733.4:p.Arg1435=