Canonical Allele Identifier: CA510467641

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024586T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436783T>C , CM000682.2:g.32436783T>C	GRCh38
NC_000020.10:g.31024586T>C , CM000682.1:g.31024586T>C	GRCh37
NC_000020.9:g.30488247T>C	NCBI36
NG_027868.1:g.83440T>C , LRG_630:g.83440T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4071T>C MANE Select	ENSP00000364839.4:p.Ala1357=
ENST00000646985.1:c.3888T>C	ENSP00000495053.1:p.Ala1296=
ENST00000647223.1:n.6424T>C
ENST00000651418.1:c.1870-1647T>C	ENSP00000499150.1:n.1870-1647T>C
ENST00000306058.9:c.4056T>C	ENSP00000305119.5:p.Ala1352=
ENST00000375687.8:c.4071T>C	ENSP00000364839.4:p.Ala1357=
ENST00000613218.4:c.4071T>C	ENSP00000480487.1:p.Ala1357=
ENST00000620121.4:c.4071T>C	ENSP00000481978.1:p.Ala1357=
NM_015338.5:c.4071T>C , LRG_630t1:c.4071T>C	NP_056153.2:p.Ala1357=
XM_006723727.2:c.4068T>C	XP_006723790.1:p.Ala1356=
XM_006723728.2:c.4041T>C	XP_006723791.1:p.Ala1347=
XM_006723730.2:c.3987T>C	XP_006723793.1:p.Ala1329=
XM_006723732.2:c.3888T>C	XP_006723795.1:p.Ala1296=
XM_006723733.1:c.3387T>C	XP_006723796.1:p.Ala1129=
XM_011528647.1:c.4335T>C	XP_011526949.1:p.Ala1445=
XM_011528648.1:c.4332T>C	XP_011526950.1:p.Ala1444=
XM_011528649.1:c.4251T>C	XP_011526951.1:p.Ala1417=
XM_011528650.1:c.4182T>C	XP_011526952.1:p.Ala1394=
XM_011528651.1:c.4050T>C	XP_011526953.1:p.Ala1350=
XM_011528652.1:c.3987T>C	XP_011526954.1:p.Ala1329=
NM_001363734.1:c.3888T>C	NP_001350663.1:p.Ala1296=
XM_006723727.3:c.4068T>C	XP_006723790.1:p.Ala1356=
XM_006723728.3:c.4041T>C	XP_006723791.1:p.Ala1347=
XM_006723730.4:c.3987T>C	XP_006723793.1:p.Ala1329=
XM_011528648.3:c.4332T>C	XP_011526950.1:p.Ala1444=
XM_011528652.2:c.3987T>C	XP_011526954.1:p.Ala1329=
XM_017027704.1:c.3987T>C	XP_016883193.1:p.Ala1329=
XM_017027705.1:c.3987T>C	XP_016883194.1:p.Ala1329=
XM_017027706.1:c.3918T>C	XP_016883195.1:p.Ala1306=
NM_015338.6:c.4071T>C MANE Select	NP_056153.2:p.Ala1357=