Canonical Allele Identifier: CA9808892

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 2902525
• ClinVar RCV Id: RCV003733804
• dbSNP Id: rs202102305
• ExAC: 20:31024270 A / G
• gnomAD v2: 20-31024270-A-G
• gnomAD v3: 20-32436467-A-G
• gnomAD v4: 20-32436467-A-G
• MyVariant Identifiers: chr20:g.31024270A>G (hg19) ; chr20:g.32436467A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436467A>G , CM000682.2:g.32436467A>G	GRCh38
NC_000020.10:g.31024270A>G , CM000682.1:g.31024270A>G	GRCh37
NC_000020.9:g.30487931A>G	NCBI36
NG_027868.1:g.83124A>G , LRG_630:g.83124A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3755A>G MANE Select	ENSP00000364839.4:p.Asp1252Gly
ENST00000646985.1:c.3572A>G	ENSP00000495053.1:p.Asp1191Gly
ENST00000647223.1:n.6108A>G
ENST00000651418.1:c.1869+1886A>G	ENSP00000499150.1:n.1869+1886A>G
ENST00000306058.9:c.3740A>G	ENSP00000305119.5:p.Asp1247Gly
ENST00000375687.8:c.3755A>G	ENSP00000364839.4:p.Asp1252Gly
ENST00000613218.4:c.3755A>G	ENSP00000480487.1:p.Asp1252Gly
ENST00000620121.4:c.3755A>G	ENSP00000481978.1:p.Asp1252Gly
NM_015338.5:c.3755A>G , LRG_630t1:c.3755A>G	NP_056153.2:p.Asp1252Gly
XM_006723727.2:c.3752A>G	XP_006723790.1:p.Asp1251Gly
XM_006723728.2:c.3725A>G	XP_006723791.1:p.Asp1242Gly
XM_006723730.2:c.3671A>G	XP_006723793.1:p.Asp1224Gly
XM_006723732.2:c.3572A>G	XP_006723795.1:p.Asp1191Gly
XM_006723733.1:c.3071A>G	XP_006723796.1:p.Asp1024Gly
XM_011528647.1:c.4019A>G	XP_011526949.1:p.Asp1340Gly
XM_011528648.1:c.4016A>G	XP_011526950.1:p.Asp1339Gly
XM_011528649.1:c.3935A>G	XP_011526951.1:p.Asp1312Gly
XM_011528650.1:c.3866A>G	XP_011526952.1:p.Asp1289Gly
XM_011528651.1:c.3734A>G	XP_011526953.1:p.Asp1245Gly
XM_011528652.1:c.3671A>G	XP_011526954.1:p.Asp1224Gly
NM_001363734.1:c.3572A>G	NP_001350663.1:p.Asp1191Gly
XM_006723727.3:c.3752A>G	XP_006723790.1:p.Asp1251Gly
XM_006723728.3:c.3725A>G	XP_006723791.1:p.Asp1242Gly
XM_006723730.4:c.3671A>G	XP_006723793.1:p.Asp1224Gly
XM_011528648.3:c.4016A>G	XP_011526950.1:p.Asp1339Gly
XM_011528652.2:c.3671A>G	XP_011526954.1:p.Asp1224Gly
XM_017027704.1:c.3671A>G	XP_016883193.1:p.Asp1224Gly
XM_017027705.1:c.3671A>G	XP_016883194.1:p.Asp1224Gly
XM_017027706.1:c.3602A>G	XP_016883195.1:p.Asp1201Gly
NM_015338.6:c.3755A>G MANE Select	NP_056153.2:p.Asp1252Gly