Canonical Allele Identifier: CA346073773

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742181-C-T
• MyVariant Identifiers: chr2:g.25965050C>T (hg19) ; chr2:g.25742181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742181C>T , CM000664.2:g.25742181C>T	GRCh38
NC_000002.11:g.25965050C>T , CM000664.1:g.25965050C>T	GRCh37
NC_000002.10:g.25818554C>T	NCBI36
NG_052995.1:g.141336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4153G>A	ENSP00000337250.5:p.Ala1385Thr
ENST00000435504.9:c.4156G>A MANE Select	ENSP00000391447.3:p.Ala1386Thr
ENST00000336112.8:c.4072G>A	ENSP00000337250.4:p.Ala1358Thr
ENST00000404843.5:c.2605G>A	ENSP00000383920.1:p.Ala869Thr
ENST00000435504.8:c.4156G>A	ENSP00000391447.3:p.Ala1386Thr
NM_018263.4:c.4156G>A	NP_060733.4:p.Ala1386Thr
XM_006712039.2:c.3790G>A	XP_006712102.1:p.Ala1264Thr
XM_006712040.1:c.3376G>A	XP_006712103.1:p.Ala1126Thr
XM_011532950.1:c.4153G>A	XP_011531252.1:p.Ala1385Thr
XM_011532951.1:c.3982G>A	XP_011531253.1:p.Ala1328Thr
NM_018263.5:c.4156G>A	NP_060733.4:p.Ala1386Thr
XM_006712039.3:c.3790G>A	XP_006712102.1:p.Ala1264Thr
XM_006712040.2:c.3376G>A	XP_006712103.1:p.Ala1126Thr
XM_011532950.3:c.4153G>A	XP_011531252.1:p.Ala1385Thr
XM_011532951.2:c.3982G>A	XP_011531253.1:p.Ala1328Thr
XM_017004430.1:c.3376G>A	XP_016859919.1:p.Ala1126Thr
XM_024452974.1:c.4336G>A	XP_024308742.1:p.Ala1446Thr
NM_001369346.1:c.3982G>A	NP_001356275.1:p.Ala1328Thr
NM_001369347.1:c.3376G>A	NP_001356276.1:p.Ala1126Thr
NM_018263.6:c.4156G>A MANE Select	NP_060733.4:p.Ala1386Thr