Canonical Allele Identifier: CA346073702

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965017G>T (hg19) ; chr2:g.25742148G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742148G>T , CM000664.2:g.25742148G>T	GRCh38
NC_000002.11:g.25965017G>T , CM000664.1:g.25965017G>T	GRCh37
NC_000002.10:g.25818521G>T	NCBI36
NG_052995.1:g.141369C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4186C>A	ENSP00000337250.5:p.Pro1396Thr
ENST00000435504.9:c.4189C>A MANE Select	ENSP00000391447.3:p.Pro1397Thr
ENST00000336112.8:c.4105C>A	ENSP00000337250.4:p.Pro1369Thr
ENST00000404843.5:c.2638C>A	ENSP00000383920.1:p.Pro880Thr
ENST00000435504.8:c.4189C>A	ENSP00000391447.3:p.Pro1397Thr
NM_018263.4:c.4189C>A	NP_060733.4:p.Pro1397Thr
XM_006712039.2:c.3823C>A	XP_006712102.1:p.Pro1275Thr
XM_006712040.1:c.3409C>A	XP_006712103.1:p.Pro1137Thr
XM_011532950.1:c.4186C>A	XP_011531252.1:p.Pro1396Thr
XM_011532951.1:c.4015C>A	XP_011531253.1:p.Pro1339Thr
NM_018263.5:c.4189C>A	NP_060733.4:p.Pro1397Thr
XM_006712039.3:c.3823C>A	XP_006712102.1:p.Pro1275Thr
XM_006712040.2:c.3409C>A	XP_006712103.1:p.Pro1137Thr
XM_011532950.3:c.4186C>A	XP_011531252.1:p.Pro1396Thr
XM_011532951.2:c.4015C>A	XP_011531253.1:p.Pro1339Thr
XM_017004430.1:c.3409C>A	XP_016859919.1:p.Pro1137Thr
XM_024452974.1:c.4369C>A	XP_024308742.1:p.Pro1457Thr
NM_001369346.1:c.4015C>A	NP_001356275.1:p.Pro1339Thr
NM_001369347.1:c.3409C>A	NP_001356276.1:p.Pro1137Thr
NM_018263.6:c.4189C>A MANE Select	NP_060733.4:p.Pro1397Thr