Canonical Allele Identifier: CA408551457

Gene: ASXL1

Linked Data

• dbSNP Id: rs2123209026
• MyVariant Identifiers: chr20:g.31015982C>A (hg19) ; chr20:g.32428179C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32428179C>A , CM000682.2:g.32428179C>A	GRCh38
NC_000020.10:g.31015982C>A , CM000682.1:g.31015982C>A	GRCh37
NC_000020.9:g.30479643C>A	NCBI36
NG_027868.1:g.74836C>A , LRG_630:g.74836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375687.10:c.304C>A MANE Select	ENSP00000364839.4:p.Pro102Thr
ENST00000470145.3:n.247C>A
ENST00000643168.1:c.220C>A	ENSP00000495003.1:p.Pro74Thr
ENST00000644060.1:n.1108C>A
ENST00000644587.1:c.*143C>A	ENSP00000494813.1:n.*143C>A
ENST00000644615.1:n.8C>A
ENST00000645514.1:n.52C>A
ENST00000645688.1:c.220C>A	ENSP00000495488.1:p.Pro74Thr
ENST00000646985.1:c.274C>A	ENSP00000495053.1:p.Pro92Thr
ENST00000651418.1:c.304C>A	ENSP00000499150.1:p.Pro102Thr
ENST00000306058.9:c.289C>A	ENSP00000305119.5:p.Pro97Thr
ENST00000375687.8:c.304C>A	ENSP00000364839.4:p.Pro102Thr
ENST00000470145.2:n.247C>A
ENST00000613218.4:c.304C>A	ENSP00000480487.1:p.Pro102Thr
ENST00000620121.4:c.304C>A	ENSP00000481978.1:p.Pro102Thr
NM_015338.5:c.304C>A , LRG_630t1:c.304C>A	NP_056153.2:p.Pro102Thr
XM_006723727.2:c.301C>A	XP_006723790.1:p.Pro101Thr
XM_006723728.2:c.274C>A	XP_006723791.1:p.Pro92Thr
XM_006723730.2:c.220C>A	XP_006723793.1:p.Pro74Thr
XM_006723732.2:c.274C>A	XP_006723795.1:p.Pro92Thr
XM_011528647.1:c.568C>A	XP_011526949.1:p.Pro190Thr
XM_011528648.1:c.565C>A	XP_011526950.1:p.Pro189Thr
XM_011528649.1:c.484C>A	XP_011526951.1:p.Pro162Thr
XM_011528650.1:c.568C>A	XP_011526952.1:p.Pro190Thr
XM_011528651.1:c.283C>A	XP_011526953.1:p.Pro95Thr
XM_011528652.1:c.220C>A	XP_011526954.1:p.Pro74Thr
NM_001363734.1:c.274C>A	NP_001350663.1:p.Pro92Thr
XM_006723727.3:c.301C>A	XP_006723790.1:p.Pro101Thr
XM_006723728.3:c.274C>A	XP_006723791.1:p.Pro92Thr
XM_006723730.4:c.220C>A	XP_006723793.1:p.Pro74Thr
XM_011528648.3:c.565C>A	XP_011526950.1:p.Pro189Thr
XM_011528652.2:c.220C>A	XP_011526954.1:p.Pro74Thr
XM_017027704.1:c.220C>A	XP_016883193.1:p.Pro74Thr
XM_017027705.1:c.220C>A	XP_016883194.1:p.Pro74Thr
XM_017027706.1:c.304C>A	XP_016883195.1:p.Pro102Thr
NM_015338.6:c.304C>A MANE Select	NP_056153.2:p.Pro102Thr