Canonical Allele Identifier: CA408564363

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436777-C-A
• MyVariant Identifiers: chr20:g.31024580C>A (hg19) ; chr20:g.32436777C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436777C>A , CM000682.2:g.32436777C>A	GRCh38
NC_000020.10:g.31024580C>A , CM000682.1:g.31024580C>A	GRCh37
NC_000020.9:g.30488241C>A	NCBI36
NG_027868.1:g.83434C>A , LRG_630:g.83434C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4065C>A MANE Select	ENSP00000364839.4:p.Asp1355Glu
ENST00000646985.1:c.3882C>A	ENSP00000495053.1:p.Asp1294Glu
ENST00000647223.1:n.6418C>A
ENST00000651418.1:c.1870-1653C>A	ENSP00000499150.1:n.1870-1653C>A
ENST00000306058.9:c.4050C>A	ENSP00000305119.5:p.Asp1350Glu
ENST00000375687.8:c.4065C>A	ENSP00000364839.4:p.Asp1355Glu
ENST00000613218.4:c.4065C>A	ENSP00000480487.1:p.Asp1355Glu
ENST00000620121.4:c.4065C>A	ENSP00000481978.1:p.Asp1355Glu
NM_015338.5:c.4065C>A , LRG_630t1:c.4065C>A	NP_056153.2:p.Asp1355Glu
XM_006723727.2:c.4062C>A	XP_006723790.1:p.Asp1354Glu
XM_006723728.2:c.4035C>A	XP_006723791.1:p.Asp1345Glu
XM_006723730.2:c.3981C>A	XP_006723793.1:p.Asp1327Glu
XM_006723732.2:c.3882C>A	XP_006723795.1:p.Asp1294Glu
XM_006723733.1:c.3381C>A	XP_006723796.1:p.Asp1127Glu
XM_011528647.1:c.4329C>A	XP_011526949.1:p.Asp1443Glu
XM_011528648.1:c.4326C>A	XP_011526950.1:p.Asp1442Glu
XM_011528649.1:c.4245C>A	XP_011526951.1:p.Asp1415Glu
XM_011528650.1:c.4176C>A	XP_011526952.1:p.Asp1392Glu
XM_011528651.1:c.4044C>A	XP_011526953.1:p.Asp1348Glu
XM_011528652.1:c.3981C>A	XP_011526954.1:p.Asp1327Glu
NM_001363734.1:c.3882C>A	NP_001350663.1:p.Asp1294Glu
XM_006723727.3:c.4062C>A	XP_006723790.1:p.Asp1354Glu
XM_006723728.3:c.4035C>A	XP_006723791.1:p.Asp1345Glu
XM_006723730.4:c.3981C>A	XP_006723793.1:p.Asp1327Glu
XM_011528648.3:c.4326C>A	XP_011526950.1:p.Asp1442Glu
XM_011528652.2:c.3981C>A	XP_011526954.1:p.Asp1327Glu
XM_017027704.1:c.3981C>A	XP_016883193.1:p.Asp1327Glu
XM_017027705.1:c.3981C>A	XP_016883194.1:p.Asp1327Glu
XM_017027706.1:c.3912C>A	XP_016883195.1:p.Asp1304Glu
NM_015338.6:c.4065C>A MANE Select	NP_056153.2:p.Asp1355Glu