Canonical Allele Identifier: CA1557328

Gene: ASXL2

Linked Data

• dbSNP Id: rs746550801
• ExAC: 2:25964961 A / T
• gnomAD v2: 2-25964961-A-T
• gnomAD v4: 2-25742092-A-T
• MyVariant Identifiers: chr2:g.25964961A>T (hg19) ; chr2:g.25742092A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742092A>T , CM000664.2:g.25742092A>T	GRCh38
NC_000002.11:g.25964961A>T , CM000664.1:g.25964961A>T	GRCh37
NC_000002.10:g.25818465A>T	NCBI36
NG_052995.1:g.141425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4242T>A	ENSP00000337250.5:p.Ala1414=
ENST00000435504.9:c.4245T>A MANE Select	ENSP00000391447.3:p.Ala1415=
ENST00000336112.8:c.4161T>A	ENSP00000337250.4:p.Ala1387=
ENST00000404843.5:c.2694T>A	ENSP00000383920.1:p.Ala898=
ENST00000435504.8:c.4245T>A	ENSP00000391447.3:p.Ala1415=
NM_018263.4:c.4245T>A	NP_060733.4:p.Ala1415=
XM_006712039.2:c.3879T>A	XP_006712102.1:p.Ala1293=
XM_006712040.1:c.3465T>A	XP_006712103.1:p.Ala1155=
XM_011532950.1:c.4242T>A	XP_011531252.1:p.Ala1414=
XM_011532951.1:c.4071T>A	XP_011531253.1:p.Ala1357=
NM_018263.5:c.4245T>A	NP_060733.4:p.Ala1415=
XM_006712039.3:c.3879T>A	XP_006712102.1:p.Ala1293=
XM_006712040.2:c.3465T>A	XP_006712103.1:p.Ala1155=
XM_011532950.3:c.4242T>A	XP_011531252.1:p.Ala1414=
XM_011532951.2:c.4071T>A	XP_011531253.1:p.Ala1357=
XM_017004430.1:c.3465T>A	XP_016859919.1:p.Ala1155=
XM_024452974.1:c.4425T>A	XP_024308742.1:p.Ala1475=
NM_001369346.1:c.4071T>A	NP_001356275.1:p.Ala1357=
NM_001369347.1:c.3465T>A	NP_001356276.1:p.Ala1155=
NM_018263.6:c.4245T>A MANE Select	NP_060733.4:p.Ala1415=