Canonical Allele Identifier: CA408562938

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023896T>G (hg19) ; chr20:g.32436093T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436093T>G , CM000682.2:g.32436093T>G	GRCh38
NC_000020.10:g.31023896T>G , CM000682.1:g.31023896T>G	GRCh37
NC_000020.9:g.30487557T>G	NCBI36
NG_027868.1:g.82750T>G , LRG_630:g.82750T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3381T>G MANE Select	ENSP00000364839.4:p.Asp1127Glu
ENST00000646985.1:c.3198T>G	ENSP00000495053.1:p.Asp1066Glu
ENST00000647223.1:n.5734T>G
ENST00000651418.1:c.1869+1512T>G	ENSP00000499150.1:n.1869+1512T>G
ENST00000306058.9:c.3366T>G	ENSP00000305119.5:p.Asp1122Glu
ENST00000375687.8:c.3381T>G	ENSP00000364839.4:p.Asp1127Glu
ENST00000613218.4:c.3381T>G	ENSP00000480487.1:p.Asp1127Glu
ENST00000620121.4:c.3381T>G	ENSP00000481978.1:p.Asp1127Glu
NM_015338.5:c.3381T>G , LRG_630t1:c.3381T>G	NP_056153.2:p.Asp1127Glu
XM_006723727.2:c.3378T>G	XP_006723790.1:p.Asp1126Glu
XM_006723728.2:c.3351T>G	XP_006723791.1:p.Asp1117Glu
XM_006723730.2:c.3297T>G	XP_006723793.1:p.Asp1099Glu
XM_006723732.2:c.3198T>G	XP_006723795.1:p.Asp1066Glu
XM_006723733.1:c.2697T>G	XP_006723796.1:p.Asp899Glu
XM_011528647.1:c.3645T>G	XP_011526949.1:p.Asp1215Glu
XM_011528648.1:c.3642T>G	XP_011526950.1:p.Asp1214Glu
XM_011528649.1:c.3561T>G	XP_011526951.1:p.Asp1187Glu
XM_011528650.1:c.3492T>G	XP_011526952.1:p.Asp1164Glu
XM_011528651.1:c.3360T>G	XP_011526953.1:p.Asp1120Glu
XM_011528652.1:c.3297T>G	XP_011526954.1:p.Asp1099Glu
NM_001363734.1:c.3198T>G	NP_001350663.1:p.Asp1066Glu
XM_006723727.3:c.3378T>G	XP_006723790.1:p.Asp1126Glu
XM_006723728.3:c.3351T>G	XP_006723791.1:p.Asp1117Glu
XM_006723730.4:c.3297T>G	XP_006723793.1:p.Asp1099Glu
XM_011528648.3:c.3642T>G	XP_011526950.1:p.Asp1214Glu
XM_011528652.2:c.3297T>G	XP_011526954.1:p.Asp1099Glu
XM_017027704.1:c.3297T>G	XP_016883193.1:p.Asp1099Glu
XM_017027705.1:c.3297T>G	XP_016883194.1:p.Asp1099Glu
XM_017027706.1:c.3228T>G	XP_016883195.1:p.Asp1076Glu
NM_015338.6:c.3381T>G MANE Select	NP_056153.2:p.Asp1127Glu