Canonical Allele Identifier: CA16620923

Gene: ASXL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435522del , CM000682.2:g.32435522del	GRCh38
NC_000020.10:g.31023325del , CM000682.1:g.31023325del	GRCh37
NC_000020.9:g.30486986del	NCBI36
NG_027868.1:g.82179del , LRG_630:g.82179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.2810del MANE Select	ENSP00000364839.4:p.Pro937LeufsTer8
ENST00000646985.1:c.2627del	ENSP00000495053.1:p.Pro876LeufsTer8
ENST00000647223.1:n.5163del
ENST00000651418.1:c.1869+941del	ENSP00000499150.1:n.1869+941del
ENST00000306058.9:c.2795del	ENSP00000305119.5:p.Pro932LeufsTer8
ENST00000375687.8:c.2810del	ENSP00000364839.4:p.Pro937LeufsTer8
ENST00000613218.4:c.2810del	ENSP00000480487.1:p.Pro937LeufsTer8
ENST00000620121.4:c.2810del	ENSP00000481978.1:p.Pro937LeufsTer8
NM_015338.5:c.2810del , LRG_630t1:c.2810del	NP_056153.2:p.Pro937LeufsTer8
XM_006723727.2:c.2807del	XP_006723790.1:p.Pro936LeufsTer8
XM_006723728.2:c.2780del	XP_006723791.1:p.Pro927LeufsTer8
XM_006723730.2:c.2726del	XP_006723793.1:p.Pro909LeufsTer8
XM_006723732.2:c.2627del	XP_006723795.1:p.Pro876LeufsTer8
XM_006723733.1:c.2126del	XP_006723796.1:p.Pro709LeufsTer8
XM_011528647.1:c.3074del	XP_011526949.1:p.Pro1025LeufsTer8
XM_011528648.1:c.3071del	XP_011526950.1:p.Pro1024LeufsTer8
XM_011528649.1:c.2990del	XP_011526951.1:p.Pro997LeufsTer8
XM_011528650.1:c.2921del	XP_011526952.1:p.Pro974LeufsTer8
XM_011528651.1:c.2789del	XP_011526953.1:p.Pro930LeufsTer8
XM_011528652.1:c.2726del	XP_011526954.1:p.Pro909LeufsTer8
NM_001363734.1:c.2627del	NP_001350663.1:p.Pro876LeufsTer8
XM_006723727.3:c.2807del	XP_006723790.1:p.Pro936LeufsTer8
XM_006723728.3:c.2780del	XP_006723791.1:p.Pro927LeufsTer8
XM_006723730.4:c.2726del	XP_006723793.1:p.Pro909LeufsTer8
XM_011528648.3:c.3071del	XP_011526950.1:p.Pro1024LeufsTer8
XM_011528652.2:c.2726del	XP_011526954.1:p.Pro909LeufsTer8
XM_017027704.1:c.2726del	XP_016883193.1:p.Pro909LeufsTer8
XM_017027705.1:c.2726del	XP_016883194.1:p.Pro909LeufsTer8
XM_017027706.1:c.2657del	XP_016883195.1:p.Pro886LeufsTer8
NM_015338.6:c.2810del MANE Select	NP_056153.2:p.Pro937LeufsTer8