Canonical Allele Identifier: CA408563195

Gene: ASXL1

Linked Data

• ClinVar Variation Id: 1475381
• ClinVar RCV Id: RCV001976195
• dbSNP Id: rs1291218446
• gnomAD v2: 20-31024017-A-C
• gnomAD v3: 20-32436214-A-C
• gnomAD v4: 20-32436214-A-C
• MyVariant Identifiers: chr20:g.31024017A>C (hg19) ; chr20:g.32436214A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436214A>C , CM000682.2:g.32436214A>C	GRCh38
NC_000020.10:g.31024017A>C , CM000682.1:g.31024017A>C	GRCh37
NC_000020.9:g.30487678A>C	NCBI36
NG_027868.1:g.82871A>C , LRG_630:g.82871A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3502A>C MANE Select	ENSP00000364839.4:p.Ser1168Arg
ENST00000646985.1:c.3319A>C	ENSP00000495053.1:p.Ser1107Arg
ENST00000647223.1:n.5855A>C
ENST00000651418.1:c.1869+1633A>C	ENSP00000499150.1:n.1869+1633A>C
ENST00000306058.9:c.3487A>C	ENSP00000305119.5:p.Ser1163Arg
ENST00000375687.8:c.3502A>C	ENSP00000364839.4:p.Ser1168Arg
ENST00000613218.4:c.3502A>C	ENSP00000480487.1:p.Ser1168Arg
ENST00000620121.4:c.3502A>C	ENSP00000481978.1:p.Ser1168Arg
NM_015338.5:c.3502A>C , LRG_630t1:c.3502A>C	NP_056153.2:p.Ser1168Arg
XM_006723727.2:c.3499A>C	XP_006723790.1:p.Ser1167Arg
XM_006723728.2:c.3472A>C	XP_006723791.1:p.Ser1158Arg
XM_006723730.2:c.3418A>C	XP_006723793.1:p.Ser1140Arg
XM_006723732.2:c.3319A>C	XP_006723795.1:p.Ser1107Arg
XM_006723733.1:c.2818A>C	XP_006723796.1:p.Ser940Arg
XM_011528647.1:c.3766A>C	XP_011526949.1:p.Ser1256Arg
XM_011528648.1:c.3763A>C	XP_011526950.1:p.Ser1255Arg
XM_011528649.1:c.3682A>C	XP_011526951.1:p.Ser1228Arg
XM_011528650.1:c.3613A>C	XP_011526952.1:p.Ser1205Arg
XM_011528651.1:c.3481A>C	XP_011526953.1:p.Ser1161Arg
XM_011528652.1:c.3418A>C	XP_011526954.1:p.Ser1140Arg
NM_001363734.1:c.3319A>C	NP_001350663.1:p.Ser1107Arg
XM_006723727.3:c.3499A>C	XP_006723790.1:p.Ser1167Arg
XM_006723728.3:c.3472A>C	XP_006723791.1:p.Ser1158Arg
XM_006723730.4:c.3418A>C	XP_006723793.1:p.Ser1140Arg
XM_011528648.3:c.3763A>C	XP_011526950.1:p.Ser1255Arg
XM_011528652.2:c.3418A>C	XP_011526954.1:p.Ser1140Arg
XM_017027704.1:c.3418A>C	XP_016883193.1:p.Ser1140Arg
XM_017027705.1:c.3418A>C	XP_016883194.1:p.Ser1140Arg
XM_017027706.1:c.3349A>C	XP_016883195.1:p.Ser1117Arg
NM_015338.6:c.3502A>C MANE Select	NP_056153.2:p.Ser1168Arg