Canonical Allele Identifier: CA510467258

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436165T>A , CM000682.2:g.32436165T>A	GRCh38
NC_000020.10:g.31023968T>A , CM000682.1:g.31023968T>A	GRCh37
NC_000020.9:g.30487629T>A	NCBI36
NG_027868.1:g.82822T>A , LRG_630:g.82822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3453T>A MANE Select	ENSP00000364839.4:p.Ser1151=
ENST00000646985.1:c.3270T>A	ENSP00000495053.1:p.Ser1090=
ENST00000647223.1:n.5806T>A
ENST00000651418.1:c.1869+1584T>A	ENSP00000499150.1:n.1869+1584T>A
ENST00000306058.9:c.3438T>A	ENSP00000305119.5:p.Ser1146=
ENST00000375687.8:c.3453T>A	ENSP00000364839.4:p.Ser1151=
ENST00000613218.4:c.3453T>A	ENSP00000480487.1:p.Ser1151=
ENST00000620121.4:c.3453T>A	ENSP00000481978.1:p.Ser1151=
NM_015338.5:c.3453T>A , LRG_630t1:c.3453T>A	NP_056153.2:p.Ser1151=
XM_006723727.2:c.3450T>A	XP_006723790.1:p.Ser1150=
XM_006723728.2:c.3423T>A	XP_006723791.1:p.Ser1141=
XM_006723730.2:c.3369T>A	XP_006723793.1:p.Ser1123=
XM_006723732.2:c.3270T>A	XP_006723795.1:p.Ser1090=
XM_006723733.1:c.2769T>A	XP_006723796.1:p.Ser923=
XM_011528647.1:c.3717T>A	XP_011526949.1:p.Ser1239=
XM_011528648.1:c.3714T>A	XP_011526950.1:p.Ser1238=
XM_011528649.1:c.3633T>A	XP_011526951.1:p.Ser1211=
XM_011528650.1:c.3564T>A	XP_011526952.1:p.Ser1188=
XM_011528651.1:c.3432T>A	XP_011526953.1:p.Ser1144=
XM_011528652.1:c.3369T>A	XP_011526954.1:p.Ser1123=
NM_001363734.1:c.3270T>A	NP_001350663.1:p.Ser1090=
XM_006723727.3:c.3450T>A	XP_006723790.1:p.Ser1150=
XM_006723728.3:c.3423T>A	XP_006723791.1:p.Ser1141=
XM_006723730.4:c.3369T>A	XP_006723793.1:p.Ser1123=
XM_011528648.3:c.3714T>A	XP_011526950.1:p.Ser1238=
XM_011528652.2:c.3369T>A	XP_011526954.1:p.Ser1123=
XM_017027704.1:c.3369T>A	XP_016883193.1:p.Ser1123=
XM_017027705.1:c.3369T>A	XP_016883194.1:p.Ser1123=
XM_017027706.1:c.3300T>A	XP_016883195.1:p.Ser1100=
NM_015338.6:c.3453T>A MANE Select	NP_056153.2:p.Ser1151=