Canonical Allele Identifier: CA408562764

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436008-C-G
• MyVariant Identifiers: chr20:g.31023811C>G (hg19) ; chr20:g.32436008C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436008C>G , CM000682.2:g.32436008C>G	GRCh38
NC_000020.10:g.31023811C>G , CM000682.1:g.31023811C>G	GRCh37
NC_000020.9:g.30487472C>G	NCBI36
NG_027868.1:g.82665C>G , LRG_630:g.82665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3296C>G MANE Select	ENSP00000364839.4:p.Ser1099Cys
ENST00000646985.1:c.3113C>G	ENSP00000495053.1:p.Ser1038Cys
ENST00000647223.1:n.5649C>G
ENST00000651418.1:c.1869+1427C>G	ENSP00000499150.1:n.1869+1427C>G
ENST00000306058.9:c.3281C>G	ENSP00000305119.5:p.Ser1094Cys
ENST00000375687.8:c.3296C>G	ENSP00000364839.4:p.Ser1099Cys
ENST00000613218.4:c.3296C>G	ENSP00000480487.1:p.Ser1099Cys
ENST00000620121.4:c.3296C>G	ENSP00000481978.1:p.Ser1099Cys
NM_015338.5:c.3296C>G , LRG_630t1:c.3296C>G	NP_056153.2:p.Ser1099Cys
XM_006723727.2:c.3293C>G	XP_006723790.1:p.Ser1098Cys
XM_006723728.2:c.3266C>G	XP_006723791.1:p.Ser1089Cys
XM_006723730.2:c.3212C>G	XP_006723793.1:p.Ser1071Cys
XM_006723732.2:c.3113C>G	XP_006723795.1:p.Ser1038Cys
XM_006723733.1:c.2612C>G	XP_006723796.1:p.Ser871Cys
XM_011528647.1:c.3560C>G	XP_011526949.1:p.Ser1187Cys
XM_011528648.1:c.3557C>G	XP_011526950.1:p.Ser1186Cys
XM_011528649.1:c.3476C>G	XP_011526951.1:p.Ser1159Cys
XM_011528650.1:c.3407C>G	XP_011526952.1:p.Ser1136Cys
XM_011528651.1:c.3275C>G	XP_011526953.1:p.Ser1092Cys
XM_011528652.1:c.3212C>G	XP_011526954.1:p.Ser1071Cys
NM_001363734.1:c.3113C>G	NP_001350663.1:p.Ser1038Cys
XM_006723727.3:c.3293C>G	XP_006723790.1:p.Ser1098Cys
XM_006723728.3:c.3266C>G	XP_006723791.1:p.Ser1089Cys
XM_006723730.4:c.3212C>G	XP_006723793.1:p.Ser1071Cys
XM_011528648.3:c.3557C>G	XP_011526950.1:p.Ser1186Cys
XM_011528652.2:c.3212C>G	XP_011526954.1:p.Ser1071Cys
XM_017027704.1:c.3212C>G	XP_016883193.1:p.Ser1071Cys
XM_017027705.1:c.3212C>G	XP_016883194.1:p.Ser1071Cys
XM_017027706.1:c.3143C>G	XP_016883195.1:p.Ser1048Cys
NM_015338.6:c.3296C>G MANE Select	NP_056153.2:p.Ser1099Cys