Canonical Allele Identifier: CA408562663

Gene: ASXL1

Linked Data

• dbSNP Id: rs2011829454
• gnomAD v4: 20-32435963-G-A
• COSMIC: COSM5857651 ; COSM5857652
• MyVariant Identifiers: chr20:g.31023766G>A (hg19) ; chr20:g.32435963G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435963G>A , CM000682.2:g.32435963G>A	GRCh38
NC_000020.10:g.31023766G>A , CM000682.1:g.31023766G>A	GRCh37
NC_000020.9:g.30487427G>A	NCBI36
NG_027868.1:g.82620G>A , LRG_630:g.82620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3251G>A MANE Select	ENSP00000364839.4:p.Ser1084Asn
ENST00000646985.1:c.3068G>A	ENSP00000495053.1:p.Ser1023Asn
ENST00000647223.1:n.5604G>A
ENST00000651418.1:c.1869+1382G>A	ENSP00000499150.1:n.1869+1382G>A
ENST00000306058.9:c.3236G>A	ENSP00000305119.5:p.Ser1079Asn
ENST00000375687.8:c.3251G>A	ENSP00000364839.4:p.Ser1084Asn
ENST00000613218.4:c.3251G>A	ENSP00000480487.1:p.Ser1084Asn
ENST00000620121.4:c.3251G>A	ENSP00000481978.1:p.Ser1084Asn
NM_015338.5:c.3251G>A , LRG_630t1:c.3251G>A	NP_056153.2:p.Ser1084Asn
XM_006723727.2:c.3248G>A	XP_006723790.1:p.Ser1083Asn
XM_006723728.2:c.3221G>A	XP_006723791.1:p.Ser1074Asn
XM_006723730.2:c.3167G>A	XP_006723793.1:p.Ser1056Asn
XM_006723732.2:c.3068G>A	XP_006723795.1:p.Ser1023Asn
XM_006723733.1:c.2567G>A	XP_006723796.1:p.Ser856Asn
XM_011528647.1:c.3515G>A	XP_011526949.1:p.Ser1172Asn
XM_011528648.1:c.3512G>A	XP_011526950.1:p.Ser1171Asn
XM_011528649.1:c.3431G>A	XP_011526951.1:p.Ser1144Asn
XM_011528650.1:c.3362G>A	XP_011526952.1:p.Ser1121Asn
XM_011528651.1:c.3230G>A	XP_011526953.1:p.Ser1077Asn
XM_011528652.1:c.3167G>A	XP_011526954.1:p.Ser1056Asn
NM_001363734.1:c.3068G>A	NP_001350663.1:p.Ser1023Asn
XM_006723727.3:c.3248G>A	XP_006723790.1:p.Ser1083Asn
XM_006723728.3:c.3221G>A	XP_006723791.1:p.Ser1074Asn
XM_006723730.4:c.3167G>A	XP_006723793.1:p.Ser1056Asn
XM_011528648.3:c.3512G>A	XP_011526950.1:p.Ser1171Asn
XM_011528652.2:c.3167G>A	XP_011526954.1:p.Ser1056Asn
XM_017027704.1:c.3167G>A	XP_016883193.1:p.Ser1056Asn
XM_017027705.1:c.3167G>A	XP_016883194.1:p.Ser1056Asn
XM_017027706.1:c.3098G>A	XP_016883195.1:p.Ser1033Asn
NM_015338.6:c.3251G>A MANE Select	NP_056153.2:p.Ser1084Asn