Canonical Allele Identifier: CA2360293831

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436720_32436721delinsGA , CM000682.2:g.32436720_32436721delinsGA	GRCh38
NC_000020.10:g.31024523_31024524delinsGA , CM000682.1:g.31024523_31024524delinsGA	GRCh37
NC_000020.9:g.30488184_30488185delinsGA	NCBI36
NG_027868.1:g.83377_83378delinsGA , LRG_630:g.83377_83378delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4008_4009delinsGA MANE Select	ENSP00000364839.4:p.Gly1336=
ENST00000646985.1:c.3825_3826delinsGA	ENSP00000495053.1:p.Gly1275=
ENST00000647223.1:n.6361_6362delinsGA
ENST00000651418.1:c.1870-1710_1870-1709delinsGA	ENSP00000499150.1:n.1870-1710_1870-1709delinsGA
ENST00000306058.9:c.3993_3994delinsGA	ENSP00000305119.5:p.Gly1331=
ENST00000375687.8:c.4008_4009delinsGA	ENSP00000364839.4:p.Gly1336=
ENST00000613218.4:c.4008_4009delinsGA	ENSP00000480487.1:p.Gly1336=
ENST00000620121.4:c.4008_4009delinsGA	ENSP00000481978.1:p.Gly1336=
NM_015338.5:c.4008_4009delinsGA , LRG_630t1:c.4008_4009delinsGA	NP_056153.2:p.Gly1336=
XM_006723727.2:c.4005_4006delinsGA	XP_006723790.1:p.Gly1335=
XM_006723728.2:c.3978_3979delinsGA	XP_006723791.1:p.Gly1326=
XM_006723730.2:c.3924_3925delinsGA	XP_006723793.1:p.Gly1308=
XM_006723732.2:c.3825_3826delinsGA	XP_006723795.1:p.Gly1275=
XM_006723733.1:c.3324_3325delinsGA	XP_006723796.1:p.Gly1108=
XM_011528647.1:c.4272_4273delinsGA	XP_011526949.1:p.Gly1424=
XM_011528648.1:c.4269_4270delinsGA	XP_011526950.1:p.Gly1423=
XM_011528649.1:c.4188_4189delinsGA	XP_011526951.1:p.Gly1396=
XM_011528650.1:c.4119_4120delinsGA	XP_011526952.1:p.Gly1373=
XM_011528651.1:c.3987_3988delinsGA	XP_011526953.1:p.Gly1329=
XM_011528652.1:c.3924_3925delinsGA	XP_011526954.1:p.Gly1308=
NM_001363734.1:c.3825_3826delinsGA	NP_001350663.1:p.Gly1275=
XM_006723727.3:c.4005_4006delinsGA	XP_006723790.1:p.Gly1335=
XM_006723728.3:c.3978_3979delinsGA	XP_006723791.1:p.Gly1326=
XM_006723730.4:c.3924_3925delinsGA	XP_006723793.1:p.Gly1308=
XM_011528648.3:c.4269_4270delinsGA	XP_011526950.1:p.Gly1423=
XM_011528652.2:c.3924_3925delinsGA	XP_011526954.1:p.Gly1308=
XM_017027704.1:c.3924_3925delinsGA	XP_016883193.1:p.Gly1308=
XM_017027705.1:c.3924_3925delinsGA	XP_016883194.1:p.Gly1308=
XM_017027706.1:c.3855_3856delinsGA	XP_016883195.1:p.Gly1285=
NM_015338.6:c.4008_4009delinsGA MANE Select	NP_056153.2:p.Gly1336=