Canonical Allele Identifier: CA346076090

Gene: ASXL2

Linked Data

• MyVariant Identifiers: chr2:g.25965421G>A (hg19) ; chr2:g.25742552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742552G>A , CM000664.2:g.25742552G>A	GRCh38
NC_000002.11:g.25965421G>A , CM000664.1:g.25965421G>A	GRCh37
NC_000002.10:g.25818925G>A	NCBI36
NG_052995.1:g.140965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3782C>T	ENSP00000337250.5:p.Ala1261Val
ENST00000435504.9:c.3785C>T MANE Select	ENSP00000391447.3:p.Ala1262Val
ENST00000336112.8:c.3701C>T	ENSP00000337250.4:p.Ala1234Val
ENST00000404843.5:c.2234C>T	ENSP00000383920.1:p.Ala745Val
ENST00000435504.8:c.3785C>T	ENSP00000391447.3:p.Ala1262Val
NM_018263.4:c.3785C>T	NP_060733.4:p.Ala1262Val
XM_006712039.2:c.3419C>T	XP_006712102.1:p.Ala1140Val
XM_006712040.1:c.3005C>T	XP_006712103.1:p.Ala1002Val
XM_011532950.1:c.3782C>T	XP_011531252.1:p.Ala1261Val
XM_011532951.1:c.3611C>T	XP_011531253.1:p.Ala1204Val
NM_018263.5:c.3785C>T	NP_060733.4:p.Ala1262Val
XM_006712039.3:c.3419C>T	XP_006712102.1:p.Ala1140Val
XM_006712040.2:c.3005C>T	XP_006712103.1:p.Ala1002Val
XM_011532950.3:c.3782C>T	XP_011531252.1:p.Ala1261Val
XM_011532951.2:c.3611C>T	XP_011531253.1:p.Ala1204Val
XM_017004430.1:c.3005C>T	XP_016859919.1:p.Ala1002Val
XM_024452974.1:c.3965C>T	XP_024308742.1:p.Ala1322Val
NM_001369346.1:c.3611C>T	NP_001356275.1:p.Ala1204Val
NM_001369347.1:c.3005C>T	NP_001356276.1:p.Ala1002Val
NM_018263.6:c.3785C>T MANE Select	NP_060733.4:p.Ala1262Val