Canonical Allele Identifier: CA9808786

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 1375225
• ClinVar RCV Id: RCV001879561
• dbSNP Id: rs771806916
• ExAC: 20:31023789 G / A
• gnomAD v2: 20-31023789-G-A
• gnomAD v3: 20-32435986-G-A
• gnomAD v4: 20-32435986-G-A
• MyVariant Identifiers: chr20:g.31023789G>A (hg19) ; chr20:g.32435986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435986G>A , CM000682.2:g.32435986G>A	GRCh38
NC_000020.10:g.31023789G>A , CM000682.1:g.31023789G>A	GRCh37
NC_000020.9:g.30487450G>A	NCBI36
NG_027868.1:g.82643G>A , LRG_630:g.82643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3274G>A MANE Select	ENSP00000364839.4:p.Val1092Met
ENST00000646985.1:c.3091G>A	ENSP00000495053.1:p.Val1031Met
ENST00000647223.1:n.5627G>A
ENST00000651418.1:c.1869+1405G>A	ENSP00000499150.1:n.1869+1405G>A
ENST00000306058.9:c.3259G>A	ENSP00000305119.5:p.Val1087Met
ENST00000375687.8:c.3274G>A	ENSP00000364839.4:p.Val1092Met
ENST00000613218.4:c.3274G>A	ENSP00000480487.1:p.Val1092Met
ENST00000620121.4:c.3274G>A	ENSP00000481978.1:p.Val1092Met
NM_015338.5:c.3274G>A , LRG_630t1:c.3274G>A	NP_056153.2:p.Val1092Met
XM_006723727.2:c.3271G>A	XP_006723790.1:p.Val1091Met
XM_006723728.2:c.3244G>A	XP_006723791.1:p.Val1082Met
XM_006723730.2:c.3190G>A	XP_006723793.1:p.Val1064Met
XM_006723732.2:c.3091G>A	XP_006723795.1:p.Val1031Met
XM_006723733.1:c.2590G>A	XP_006723796.1:p.Val864Met
XM_011528647.1:c.3538G>A	XP_011526949.1:p.Val1180Met
XM_011528648.1:c.3535G>A	XP_011526950.1:p.Val1179Met
XM_011528649.1:c.3454G>A	XP_011526951.1:p.Val1152Met
XM_011528650.1:c.3385G>A	XP_011526952.1:p.Val1129Met
XM_011528651.1:c.3253G>A	XP_011526953.1:p.Val1085Met
XM_011528652.1:c.3190G>A	XP_011526954.1:p.Val1064Met
NM_001363734.1:c.3091G>A	NP_001350663.1:p.Val1031Met
XM_006723727.3:c.3271G>A	XP_006723790.1:p.Val1091Met
XM_006723728.3:c.3244G>A	XP_006723791.1:p.Val1082Met
XM_006723730.4:c.3190G>A	XP_006723793.1:p.Val1064Met
XM_011528648.3:c.3535G>A	XP_011526950.1:p.Val1179Met
XM_011528652.2:c.3190G>A	XP_011526954.1:p.Val1064Met
XM_017027704.1:c.3190G>A	XP_016883193.1:p.Val1064Met
XM_017027705.1:c.3190G>A	XP_016883194.1:p.Val1064Met
XM_017027706.1:c.3121G>A	XP_016883195.1:p.Val1041Met
NM_015338.6:c.3274G>A MANE Select	NP_056153.2:p.Val1092Met