Canonical Allele Identifier: CA510467073

Gene: ASXL1

Linked Data

• dbSNP Id: rs2145378644
• MyVariant Identifiers: chr20:g.31023713G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435910G>A , CM000682.2:g.32435910G>A	GRCh38
NC_000020.10:g.31023713G>A , CM000682.1:g.31023713G>A	GRCh37
NC_000020.9:g.30487374G>A	NCBI36
NG_027868.1:g.82567G>A , LRG_630:g.82567G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3198G>A MANE Select	ENSP00000364839.4:p.Val1066=
ENST00000646985.1:c.3015G>A	ENSP00000495053.1:p.Val1005=
ENST00000647223.1:n.5551G>A
ENST00000651418.1:c.1869+1329G>A	ENSP00000499150.1:n.1869+1329G>A
ENST00000306058.9:c.3183G>A	ENSP00000305119.5:p.Val1061=
ENST00000375687.8:c.3198G>A	ENSP00000364839.4:p.Val1066=
ENST00000613218.4:c.3198G>A	ENSP00000480487.1:p.Val1066=
ENST00000620121.4:c.3198G>A	ENSP00000481978.1:p.Val1066=
NM_015338.5:c.3198G>A , LRG_630t1:c.3198G>A	NP_056153.2:p.Val1066=
XM_006723727.2:c.3195G>A	XP_006723790.1:p.Val1065=
XM_006723728.2:c.3168G>A	XP_006723791.1:p.Val1056=
XM_006723730.2:c.3114G>A	XP_006723793.1:p.Val1038=
XM_006723732.2:c.3015G>A	XP_006723795.1:p.Val1005=
XM_006723733.1:c.2514G>A	XP_006723796.1:p.Val838=
XM_011528647.1:c.3462G>A	XP_011526949.1:p.Val1154=
XM_011528648.1:c.3459G>A	XP_011526950.1:p.Val1153=
XM_011528649.1:c.3378G>A	XP_011526951.1:p.Val1126=
XM_011528650.1:c.3309G>A	XP_011526952.1:p.Val1103=
XM_011528651.1:c.3177G>A	XP_011526953.1:p.Val1059=
XM_011528652.1:c.3114G>A	XP_011526954.1:p.Val1038=
NM_001363734.1:c.3015G>A	NP_001350663.1:p.Val1005=
XM_006723727.3:c.3195G>A	XP_006723790.1:p.Val1065=
XM_006723728.3:c.3168G>A	XP_006723791.1:p.Val1056=
XM_006723730.4:c.3114G>A	XP_006723793.1:p.Val1038=
XM_011528648.3:c.3459G>A	XP_011526950.1:p.Val1153=
XM_011528652.2:c.3114G>A	XP_011526954.1:p.Val1038=
XM_017027704.1:c.3114G>A	XP_016883193.1:p.Val1038=
XM_017027705.1:c.3114G>A	XP_016883194.1:p.Val1038=
XM_017027706.1:c.3045G>A	XP_016883195.1:p.Val1015=
NM_015338.6:c.3198G>A MANE Select	NP_056153.2:p.Val1066=