Canonical Allele Identifier: CA408562757

Gene: ASXL1

Linked Data

• MyVariant Identifiers: chr20:g.31023808G>T (hg19) ; chr20:g.32436005G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32436005G>T , CM000682.2:g.32436005G>T	GRCh38
NC_000020.10:g.31023808G>T , CM000682.1:g.31023808G>T	GRCh37
NC_000020.9:g.30487469G>T	NCBI36
NG_027868.1:g.82662G>T , LRG_630:g.82662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.3293G>T MANE Select	ENSP00000364839.4:p.Gly1098Val
ENST00000646985.1:c.3110G>T	ENSP00000495053.1:p.Gly1037Val
ENST00000647223.1:n.5646G>T
ENST00000651418.1:c.1869+1424G>T	ENSP00000499150.1:n.1869+1424G>T
ENST00000306058.9:c.3278G>T	ENSP00000305119.5:p.Gly1093Val
ENST00000375687.8:c.3293G>T	ENSP00000364839.4:p.Gly1098Val
ENST00000613218.4:c.3293G>T	ENSP00000480487.1:p.Gly1098Val
ENST00000620121.4:c.3293G>T	ENSP00000481978.1:p.Gly1098Val
NM_015338.5:c.3293G>T , LRG_630t1:c.3293G>T	NP_056153.2:p.Gly1098Val
XM_006723727.2:c.3290G>T	XP_006723790.1:p.Gly1097Val
XM_006723728.2:c.3263G>T	XP_006723791.1:p.Gly1088Val
XM_006723730.2:c.3209G>T	XP_006723793.1:p.Gly1070Val
XM_006723732.2:c.3110G>T	XP_006723795.1:p.Gly1037Val
XM_006723733.1:c.2609G>T	XP_006723796.1:p.Gly870Val
XM_011528647.1:c.3557G>T	XP_011526949.1:p.Gly1186Val
XM_011528648.1:c.3554G>T	XP_011526950.1:p.Gly1185Val
XM_011528649.1:c.3473G>T	XP_011526951.1:p.Gly1158Val
XM_011528650.1:c.3404G>T	XP_011526952.1:p.Gly1135Val
XM_011528651.1:c.3272G>T	XP_011526953.1:p.Gly1091Val
XM_011528652.1:c.3209G>T	XP_011526954.1:p.Gly1070Val
NM_001363734.1:c.3110G>T	NP_001350663.1:p.Gly1037Val
XM_006723727.3:c.3290G>T	XP_006723790.1:p.Gly1097Val
XM_006723728.3:c.3263G>T	XP_006723791.1:p.Gly1088Val
XM_006723730.4:c.3209G>T	XP_006723793.1:p.Gly1070Val
XM_011528648.3:c.3554G>T	XP_011526950.1:p.Gly1185Val
XM_011528652.2:c.3209G>T	XP_011526954.1:p.Gly1070Val
XM_017027704.1:c.3209G>T	XP_016883193.1:p.Gly1070Val
XM_017027705.1:c.3209G>T	XP_016883194.1:p.Gly1070Val
XM_017027706.1:c.3140G>T	XP_016883195.1:p.Gly1047Val
NM_015338.6:c.3293G>T MANE Select	NP_056153.2:p.Gly1098Val