Canonical Allele Identifier: CA510467609

Gene: ASXL1

Linked Data

• gnomAD v4: 20-32436769-A-C
• MyVariant Identifiers: chr20:g.31024572A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436769A>C , CM000682.2:g.32436769A>C	GRCh38
NC_000020.10:g.31024572A>C , CM000682.1:g.31024572A>C	GRCh37
NC_000020.9:g.30488233A>C	NCBI36
NG_027868.1:g.83426A>C , LRG_630:g.83426A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.4057A>C MANE Select	ENSP00000364839.4:p.Arg1353=
ENST00000646985.1:c.3874A>C	ENSP00000495053.1:p.Arg1292=
ENST00000647223.1:n.6410A>C
ENST00000651418.1:c.1870-1661A>C	ENSP00000499150.1:n.1870-1661A>C
ENST00000306058.9:c.4042A>C	ENSP00000305119.5:p.Arg1348=
ENST00000375687.8:c.4057A>C	ENSP00000364839.4:p.Arg1353=
ENST00000613218.4:c.4057A>C	ENSP00000480487.1:p.Arg1353=
ENST00000620121.4:c.4057A>C	ENSP00000481978.1:p.Arg1353=
NM_015338.5:c.4057A>C , LRG_630t1:c.4057A>C	NP_056153.2:p.Arg1353=
XM_006723727.2:c.4054A>C	XP_006723790.1:p.Arg1352=
XM_006723728.2:c.4027A>C	XP_006723791.1:p.Arg1343=
XM_006723730.2:c.3973A>C	XP_006723793.1:p.Arg1325=
XM_006723732.2:c.3874A>C	XP_006723795.1:p.Arg1292=
XM_006723733.1:c.3373A>C	XP_006723796.1:p.Arg1125=
XM_011528647.1:c.4321A>C	XP_011526949.1:p.Arg1441=
XM_011528648.1:c.4318A>C	XP_011526950.1:p.Arg1440=
XM_011528649.1:c.4237A>C	XP_011526951.1:p.Arg1413=
XM_011528650.1:c.4168A>C	XP_011526952.1:p.Arg1390=
XM_011528651.1:c.4036A>C	XP_011526953.1:p.Arg1346=
XM_011528652.1:c.3973A>C	XP_011526954.1:p.Arg1325=
NM_001363734.1:c.3874A>C	NP_001350663.1:p.Arg1292=
XM_006723727.3:c.4054A>C	XP_006723790.1:p.Arg1352=
XM_006723728.3:c.4027A>C	XP_006723791.1:p.Arg1343=
XM_006723730.4:c.3973A>C	XP_006723793.1:p.Arg1325=
XM_011528648.3:c.4318A>C	XP_011526950.1:p.Arg1440=
XM_011528652.2:c.3973A>C	XP_011526954.1:p.Arg1325=
XM_017027704.1:c.3973A>C	XP_016883193.1:p.Arg1325=
XM_017027705.1:c.3973A>C	XP_016883194.1:p.Arg1325=
XM_017027706.1:c.3904A>C	XP_016883195.1:p.Arg1302=
NM_015338.6:c.4057A>C MANE Select	NP_056153.2:p.Arg1353=