Canonical Allele Identifier: CA408562501

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023685A>T (hg19) ; chr20:g.32435882A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32435882A>T , CM000682.2:g.32435882A>T	GRCh38
NC_000020.10:g.31023685A>T , CM000682.1:g.31023685A>T	GRCh37
NC_000020.9:g.30487346A>T	NCBI36
NG_027868.1:g.82539A>T , LRG_630:g.82539A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3170A>T MANE Select	ENSP00000364839.4:p.Asp1057Val
ENST00000646985.1:c.2987A>T	ENSP00000495053.1:p.Asp996Val
ENST00000647223.1:n.5523A>T
ENST00000651418.1:c.1869+1301A>T	ENSP00000499150.1:n.1869+1301A>T
ENST00000306058.9:c.3155A>T	ENSP00000305119.5:p.Asp1052Val
ENST00000375687.8:c.3170A>T	ENSP00000364839.4:p.Asp1057Val
ENST00000613218.4:c.3170A>T	ENSP00000480487.1:p.Asp1057Val
ENST00000620121.4:c.3170A>T	ENSP00000481978.1:p.Asp1057Val
NM_015338.5:c.3170A>T , LRG_630t1:c.3170A>T	NP_056153.2:p.Asp1057Val
XM_006723727.2:c.3167A>T	XP_006723790.1:p.Asp1056Val
XM_006723728.2:c.3140A>T	XP_006723791.1:p.Asp1047Val
XM_006723730.2:c.3086A>T	XP_006723793.1:p.Asp1029Val
XM_006723732.2:c.2987A>T	XP_006723795.1:p.Asp996Val
XM_006723733.1:c.2486A>T	XP_006723796.1:p.Asp829Val
XM_011528647.1:c.3434A>T	XP_011526949.1:p.Asp1145Val
XM_011528648.1:c.3431A>T	XP_011526950.1:p.Asp1144Val
XM_011528649.1:c.3350A>T	XP_011526951.1:p.Asp1117Val
XM_011528650.1:c.3281A>T	XP_011526952.1:p.Asp1094Val
XM_011528651.1:c.3149A>T	XP_011526953.1:p.Asp1050Val
XM_011528652.1:c.3086A>T	XP_011526954.1:p.Asp1029Val
NM_001363734.1:c.2987A>T	NP_001350663.1:p.Asp996Val
XM_006723727.3:c.3167A>T	XP_006723790.1:p.Asp1056Val
XM_006723728.3:c.3140A>T	XP_006723791.1:p.Asp1047Val
XM_006723730.4:c.3086A>T	XP_006723793.1:p.Asp1029Val
XM_011528648.3:c.3431A>T	XP_011526950.1:p.Asp1144Val
XM_011528652.2:c.3086A>T	XP_011526954.1:p.Asp1029Val
XM_017027704.1:c.3086A>T	XP_016883193.1:p.Asp1029Val
XM_017027705.1:c.3086A>T	XP_016883194.1:p.Asp1029Val
XM_017027706.1:c.3017A>T	XP_016883195.1:p.Asp1006Val
NM_015338.6:c.3170A>T MANE Select	NP_056153.2:p.Asp1057Val