Canonical Allele Identifier: CA408563489

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31024156A>G (hg19) ; chr20:g.32436353A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436353A>G , CM000682.2:g.32436353A>G	GRCh38
NC_000020.10:g.31024156A>G , CM000682.1:g.31024156A>G	GRCh37
NC_000020.9:g.30487817A>G	NCBI36
NG_027868.1:g.83010A>G , LRG_630:g.83010A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375687.10:c.3641A>G MANE Select	ENSP00000364839.4:p.His1214Arg
ENST00000646985.1:c.3458A>G	ENSP00000495053.1:p.His1153Arg
ENST00000647223.1:n.5994A>G
ENST00000651418.1:c.1869+1772A>G	ENSP00000499150.1:n.1869+1772A>G
ENST00000306058.9:c.3626A>G	ENSP00000305119.5:p.His1209Arg
ENST00000375687.8:c.3641A>G	ENSP00000364839.4:p.His1214Arg
ENST00000613218.4:c.3641A>G	ENSP00000480487.1:p.His1214Arg
ENST00000620121.4:c.3641A>G	ENSP00000481978.1:p.His1214Arg
NM_015338.5:c.3641A>G , LRG_630t1:c.3641A>G	NP_056153.2:p.His1214Arg
XM_006723727.2:c.3638A>G	XP_006723790.1:p.His1213Arg
XM_006723728.2:c.3611A>G	XP_006723791.1:p.His1204Arg
XM_006723730.2:c.3557A>G	XP_006723793.1:p.His1186Arg
XM_006723732.2:c.3458A>G	XP_006723795.1:p.His1153Arg
XM_006723733.1:c.2957A>G	XP_006723796.1:p.His986Arg
XM_011528647.1:c.3905A>G	XP_011526949.1:p.His1302Arg
XM_011528648.1:c.3902A>G	XP_011526950.1:p.His1301Arg
XM_011528649.1:c.3821A>G	XP_011526951.1:p.His1274Arg
XM_011528650.1:c.3752A>G	XP_011526952.1:p.His1251Arg
XM_011528651.1:c.3620A>G	XP_011526953.1:p.His1207Arg
XM_011528652.1:c.3557A>G	XP_011526954.1:p.His1186Arg
NM_001363734.1:c.3458A>G	NP_001350663.1:p.His1153Arg
XM_006723727.3:c.3638A>G	XP_006723790.1:p.His1213Arg
XM_006723728.3:c.3611A>G	XP_006723791.1:p.His1204Arg
XM_006723730.4:c.3557A>G	XP_006723793.1:p.His1186Arg
XM_011528648.3:c.3902A>G	XP_011526950.1:p.His1301Arg
XM_011528652.2:c.3557A>G	XP_011526954.1:p.His1186Arg
XM_017027704.1:c.3557A>G	XP_016883193.1:p.His1186Arg
XM_017027705.1:c.3557A>G	XP_016883194.1:p.His1186Arg
XM_017027706.1:c.3488A>G	XP_016883195.1:p.His1163Arg
NM_015338.6:c.3641A>G MANE Select	NP_056153.2:p.His1214Arg