Canonical Allele Identifier: CA510467572

Gene: ASXL1

Linked Data

• COSMIC: COSM3840740 ; COSM3840741
• MyVariant Identifiers: chr20:g.31024523G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436720G>A , CM000682.2:g.32436720G>A	GRCh38
NC_000020.10:g.31024523G>A , CM000682.1:g.31024523G>A	GRCh37
NC_000020.9:g.30488184G>A	NCBI36
NG_027868.1:g.83377G>A , LRG_630:g.83377G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4008G>A MANE Select	ENSP00000364839.4:p.Gly1336=
ENST00000646985.1:c.3825G>A	ENSP00000495053.1:p.Gly1275=
ENST00000647223.1:n.6361G>A
ENST00000651418.1:c.1870-1710G>A	ENSP00000499150.1:n.1870-1710G>A
ENST00000306058.9:c.3993G>A	ENSP00000305119.5:p.Gly1331=
ENST00000375687.8:c.4008G>A	ENSP00000364839.4:p.Gly1336=
ENST00000613218.4:c.4008G>A	ENSP00000480487.1:p.Gly1336=
ENST00000620121.4:c.4008G>A	ENSP00000481978.1:p.Gly1336=
NM_015338.5:c.4008G>A , LRG_630t1:c.4008G>A	NP_056153.2:p.Gly1336=
XM_006723727.2:c.4005G>A	XP_006723790.1:p.Gly1335=
XM_006723728.2:c.3978G>A	XP_006723791.1:p.Gly1326=
XM_006723730.2:c.3924G>A	XP_006723793.1:p.Gly1308=
XM_006723732.2:c.3825G>A	XP_006723795.1:p.Gly1275=
XM_006723733.1:c.3324G>A	XP_006723796.1:p.Gly1108=
XM_011528647.1:c.4272G>A	XP_011526949.1:p.Gly1424=
XM_011528648.1:c.4269G>A	XP_011526950.1:p.Gly1423=
XM_011528649.1:c.4188G>A	XP_011526951.1:p.Gly1396=
XM_011528650.1:c.4119G>A	XP_011526952.1:p.Gly1373=
XM_011528651.1:c.3987G>A	XP_011526953.1:p.Gly1329=
XM_011528652.1:c.3924G>A	XP_011526954.1:p.Gly1308=
NM_001363734.1:c.3825G>A	NP_001350663.1:p.Gly1275=
XM_006723727.3:c.4005G>A	XP_006723790.1:p.Gly1335=
XM_006723728.3:c.3978G>A	XP_006723791.1:p.Gly1326=
XM_006723730.4:c.3924G>A	XP_006723793.1:p.Gly1308=
XM_011528648.3:c.4269G>A	XP_011526950.1:p.Gly1423=
XM_011528652.2:c.3924G>A	XP_011526954.1:p.Gly1308=
XM_017027704.1:c.3924G>A	XP_016883193.1:p.Gly1308=
XM_017027705.1:c.3924G>A	XP_016883194.1:p.Gly1308=
XM_017027706.1:c.3855G>A	XP_016883195.1:p.Gly1285=
NM_015338.6:c.4008G>A MANE Select	NP_056153.2:p.Gly1336=