Canonical Allele Identifier: CA743608501

Gene: ASXL1

Linked Data

• dbSNP Id: rs35966674
• gnomAD v3: 20-32428652-CTTTTT-C
• gnomAD v4: 20-32428652-CTTTTT-C
• MyVariant Identifiers: chr20:g.31016456_31016460del (hg19) ; chr20:g.32428653_32428657del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428675_32428679del , CM000682.2:g.32428675_32428679del	GRCh38
NC_000020.10:g.31016478_31016482del , CM000682.1:g.31016478_31016482del	GRCh37
NC_000020.9:g.30480139_30480143del	NCBI36
NG_027868.1:g.75332_75336del , LRG_630:g.75332_75336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.471+253_471+257del MANE Select	ENSP00000364839.4:n.471+253_471+257del
ENST00000470145.3:n.490+253_490+257del
ENST00000643168.1:c.387+253_387+257del	ENSP00000495003.1:n.387+253_387+257del
ENST00000644587.1:c.*310+253_*310+257del	ENSP00000494813.1:n.*310+253_*310+257del
ENST00000644615.1:n.175+253_175+257del
ENST00000645514.1:n.295+253_295+257del
ENST00000646985.1:c.441+253_441+257del	ENSP00000495053.1:n.441+253_441+257del
ENST00000651418.1:c.471+253_471+257del	ENSP00000499150.1:n.471+253_471+257del
ENST00000306058.9:c.456+253_456+257del	ENSP00000305119.5:n.456+253_456+257del
ENST00000375687.8:c.471+253_471+257del	ENSP00000364839.4:n.471+253_471+257del
ENST00000470145.2:n.490+253_490+257del
ENST00000613218.4:c.471+253_471+257del	ENSP00000480487.1:n.471+253_471+257del
ENST00000620121.4:c.471+253_471+257del	ENSP00000481978.1:n.471+253_471+257del
NM_015338.5:c.471+253_471+257del , LRG_630t1:c.471+253_471+257del	NP_056153.2:n.471+253_471+257del
XM_006723727.2:c.468+253_468+257del	XP_006723790.1:n.468+253_468+257del
XM_006723728.2:c.441+253_441+257del	XP_006723791.1:n.441+253_441+257del
XM_006723730.2:c.387+253_387+257del	XP_006723793.1:n.387+253_387+257del
XM_006723732.2:c.441+253_441+257del	XP_006723795.1:n.441+253_441+257del
XM_011528647.1:c.735+253_735+257del	XP_011526949.1:n.735+253_735+257del
XM_011528648.1:c.732+253_732+257del	XP_011526950.1:n.732+253_732+257del
XM_011528649.1:c.651+253_651+257del	XP_011526951.1:n.651+253_651+257del
XM_011528650.1:c.735+253_735+257del	XP_011526952.1:n.735+253_735+257del
XM_011528651.1:c.450+253_450+257del	XP_011526953.1:n.450+253_450+257del
XM_011528652.1:c.387+253_387+257del	XP_011526954.1:n.387+253_387+257del
NM_001363734.1:c.441+253_441+257del	NP_001350663.1:n.441+253_441+257del
XM_006723727.3:c.468+253_468+257del	XP_006723790.1:n.468+253_468+257del
XM_006723728.3:c.441+253_441+257del	XP_006723791.1:n.441+253_441+257del
XM_006723730.4:c.387+253_387+257del	XP_006723793.1:n.387+253_387+257del
XM_011528648.3:c.732+253_732+257del	XP_011526950.1:n.732+253_732+257del
XM_011528652.2:c.387+253_387+257del	XP_011526954.1:n.387+253_387+257del
XM_017027704.1:c.387+253_387+257del	XP_016883193.1:n.387+253_387+257del
XM_017027705.1:c.387+253_387+257del	XP_016883194.1:n.387+253_387+257del
XM_017027706.1:c.471+253_471+257del	XP_016883195.1:n.471+253_471+257del
NM_015338.6:c.471+253_471+257del MANE Select	NP_056153.2:n.471+253_471+257del