Canonical Allele Identifier: CA2816136683

Gene: ASXL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428678_32428679insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.2:g.32428678_32428679insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000020.10:g.31016481_31016482insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.1:g.31016481_31016482insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000020.9:g.30480142_30480143insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_027868.1:g.75335_75336insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_630:g.75335_75336insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000364839.4:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000470145.3:n.490+256_490+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000643168.1:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000495003.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000644587.1:c.*310+256_*310+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000494813.1:n.*310+256_*310+257insGTTTTTGTTTTTTTTTTTTTT...
ENST00000644615.1:n.175+256_175+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000645514.1:n.295+256_295+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000646985.1:c.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000495053.1:n.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000651418.1:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000499150.1:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000306058.9:c.456+256_456+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000305119.5:n.456+256_456+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000375687.8:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000364839.4:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000470145.2:n.490+256_490+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000613218.4:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000480487.1:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTT...
ENST00000620121.4:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000481978.1:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTT...
NM_015338.5:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_630t1:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_056153.2:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTT...
XM_006723727.2:c.468+256_468+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723790.1:n.468+256_468+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723728.2:c.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723791.1:n.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723730.2:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723793.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723732.2:c.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723795.1:n.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528647.1:c.735+256_735+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526949.1:n.735+256_735+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528648.1:c.732+256_732+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526950.1:n.732+256_732+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528649.1:c.651+256_651+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526951.1:n.651+256_651+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528650.1:c.735+256_735+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526952.1:n.735+256_735+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528651.1:c.450+256_450+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526953.1:n.450+256_450+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528652.1:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526954.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
NM_001363734.1:c.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001350663.1:n.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723727.3:c.468+256_468+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723790.1:n.468+256_468+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723728.3:c.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723791.1:n.441+256_441+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_006723730.4:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006723793.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528648.3:c.732+256_732+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526950.1:n.732+256_732+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_011528652.2:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011526954.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_017027704.1:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016883193.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_017027705.1:c.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016883194.1:n.387+256_387+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
XM_017027706.1:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016883195.1:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTT...
NM_015338.6:c.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_056153.2:n.471+256_471+257insGTTTTTGTTTTTTTTTTTTTTTTTTTTTT...