Canonical Allele Identifier: CA313926349

Gene: ASXL1

Linked Data

• dbSNP Id: rs534306009
• gnomAD v3: 20-32436253-A-C
• gnomAD v4: 20-32436253-A-C
• MyVariant Identifiers: chr20:g.31024056A>C (hg19) ; chr20:g.32436253A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436253A>C , CM000682.2:g.32436253A>C	GRCh38
NC_000020.10:g.31024056A>C , CM000682.1:g.31024056A>C	GRCh37
NC_000020.9:g.30487717A>C	NCBI36
NG_027868.1:g.82910A>C , LRG_630:g.82910A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3541A>C MANE Select	ENSP00000364839.4:p.Ser1181Arg
ENST00000646985.1:c.3358A>C	ENSP00000495053.1:p.Ser1120Arg
ENST00000647223.1:n.5894A>C
ENST00000651418.1:c.1869+1672A>C	ENSP00000499150.1:n.1869+1672A>C
ENST00000306058.9:c.3526A>C	ENSP00000305119.5:p.Ser1176Arg
ENST00000375687.8:c.3541A>C	ENSP00000364839.4:p.Ser1181Arg
ENST00000613218.4:c.3541A>C	ENSP00000480487.1:p.Ser1181Arg
ENST00000620121.4:c.3541A>C	ENSP00000481978.1:p.Ser1181Arg
NM_015338.5:c.3541A>C , LRG_630t1:c.3541A>C	NP_056153.2:p.Ser1181Arg
XM_006723727.2:c.3538A>C	XP_006723790.1:p.Ser1180Arg
XM_006723728.2:c.3511A>C	XP_006723791.1:p.Ser1171Arg
XM_006723730.2:c.3457A>C	XP_006723793.1:p.Ser1153Arg
XM_006723732.2:c.3358A>C	XP_006723795.1:p.Ser1120Arg
XM_006723733.1:c.2857A>C	XP_006723796.1:p.Ser953Arg
XM_011528647.1:c.3805A>C	XP_011526949.1:p.Ser1269Arg
XM_011528648.1:c.3802A>C	XP_011526950.1:p.Ser1268Arg
XM_011528649.1:c.3721A>C	XP_011526951.1:p.Ser1241Arg
XM_011528650.1:c.3652A>C	XP_011526952.1:p.Ser1218Arg
XM_011528651.1:c.3520A>C	XP_011526953.1:p.Ser1174Arg
XM_011528652.1:c.3457A>C	XP_011526954.1:p.Ser1153Arg
NM_001363734.1:c.3358A>C	NP_001350663.1:p.Ser1120Arg
XM_006723727.3:c.3538A>C	XP_006723790.1:p.Ser1180Arg
XM_006723728.3:c.3511A>C	XP_006723791.1:p.Ser1171Arg
XM_006723730.4:c.3457A>C	XP_006723793.1:p.Ser1153Arg
XM_011528648.3:c.3802A>C	XP_011526950.1:p.Ser1268Arg
XM_011528652.2:c.3457A>C	XP_011526954.1:p.Ser1153Arg
XM_017027704.1:c.3457A>C	XP_016883193.1:p.Ser1153Arg
XM_017027705.1:c.3457A>C	XP_016883194.1:p.Ser1153Arg
XM_017027706.1:c.3388A>C	XP_016883195.1:p.Ser1130Arg
NM_015338.6:c.3541A>C MANE Select	NP_056153.2:p.Ser1181Arg